Linked Data
dbSNP Id:
rs2044940464
gnomAD v3:
22-40364897-C-A
gnomAD v4:
22-40364897-C-A
MyVariant Identifiers:
chr22:g.40760901C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.40364897C>A , CM000684.2:g.40364897C>A | GRCh38 |
| NC_000022.10:g.40760901C>A , CM000684.1:g.40760901C>A | GRCh37 |
| NC_000022.9:g.39090847C>A | NCBI36 |
| NG_007993.1:g.23398C>A | |
| NG_007993.2:g.23398C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000480775.3:c.*603C>A | ENSP00000485462.2:n.*603C>A | |
| ENST00000623287.4:c.*634C>A | ENSP00000485437.1:n.*634C>A | |
| ENST00000623632.4:c.900C>A | ENSP00000485288.2:p.Ile300= | |
| ENST00000625194.4:c.1251C>A | ENSP00000485289.2:p.Ile417= | |
| ENST00000636433.1:n.1231C>A | ||
| ENST00000636714.1:c.1209C>A | ENSP00000490946.1:p.Ile403= | |
| ENST00000637666.2:c.1191+532C>A | ENSP00000489696.2:n.1191+532C>A | |
| ENST00000637669.1:c.1209C>A | ENSP00000489728.1:p.Ile403= | |
| ENST00000639722.1:c.*905C>A | ENSP00000492828.1:n.*905C>A | |
| ENST00000674592.1:n.2723C>A | ||
| ENST00000675622.1:n.4276C>A | ||
| ENST00000679609.1:c.*819C>A | ENSP00000506592.1:n.*819C>A | |
| ENST00000679656.1:n.1894C>A | ||
| ENST00000679723.1:c.1164C>A | ENSP00000505155.1:p.Ile388= | |
| ENST00000679845.1:n.1517C>A | ||
| ENST00000679904.1:n.1605C>A | ||
| ENST00000680378.1:c.1296C>A | ENSP00000505556.1:p.Ile432= | |
| ENST00000680444.1:c.*572C>A | ENSP00000505298.1:n.*572C>A | |
| ENST00000680978.1:c.1209C>A | ENSP00000505244.1:p.Ile403= | |
| ENST00000681003.1:n.672C>A | ||
| ENST00000681159.1:n.2613C>A | ||
| ENST00000216194.11:c.1251C>A | ENSP00000216194.8:p.Ile417= | |
| ENST00000342312.9:c.1191+532C>A | ENSP00000341429.6:n.1191+532C>A | |
| ENST00000623063.3:c.1209C>A MANE Select | ENSP00000485525.1:p.Ile403= | |
| ENST00000623387.1:n.340C>A | ||
| ENST00000625194.3:c.838C>A | ||
| NM_000026.2:c.1209C>A | NP_000017.1:p.Ile403= | |
| NM_001123378.1:c.1191+532C>A | NP_001116850.1:n.1191+532C>A | |
| XM_011529976.1:c.1209C>A | XP_011528278.1:p.Ile403= | |
| XM_011529977.1:c.1209C>A | XP_011528279.1:p.Ile403= | |
| XM_011529978.1:c.1191+532C>A | XP_011528280.1:n.1191+532C>A | |
| XM_011529979.1:c.1209C>A | XP_011528281.1:p.Ile403= | |
| XM_011529980.1:c.1191+532C>A | XP_011528282.1:n.1191+532C>A | |
| XM_011529981.1:c.744C>A | XP_011528283.1:p.Ile248= | |
| XM_011529982.1:c.378C>A | XP_011528284.1:p.Ile126= | |
| XR_937824.1:n.1299C>A | ||
| XR_937825.1:n.1281+532C>A | ||
| NM_000026.3:c.1209C>A | NP_000017.1:p.Ile403= | |
| NM_001123378.2:c.1191+532C>A | NP_001116850.1:n.1191+532C>A | |
| NM_001317923.1:c.1017C>A | NP_001304852.1:p.Ile339= | |
| NM_001363840.1:c.1209C>A | NP_001350769.1:p.Ile403= | |
| NR_134256.1:n.1299C>A | ||
| XM_011529977.3:c.1209C>A | XP_011528279.1:p.Ile403= | |
| XM_011529980.3:c.1191+532C>A | XP_011528282.1:n.1191+532C>A | |
| XM_017028636.1:c.1164C>A | XP_016884125.1:p.Ile388= | |
| XM_017028637.1:c.1164C>A | XP_016884126.1:p.Ile388= | |
| XM_017028638.1:c.744C>A | XP_016884127.1:p.Ile248= | |
| XM_017028639.2:c.744C>A | XP_016884128.1:p.Ile248= | |
| XM_017028640.1:c.378C>A | XP_016884129.1:p.Ile126= | |
| XM_024452166.1:c.1146+532C>A | XP_024307934.1:n.1146+532C>A | |
| XR_001755176.2:n.1451C>A | ||
| XR_002958670.1:n.1236C>A | ||
| XR_937825.3:n.1279+532C>A | ||
| NM_000026.4:c.1209C>A MANE Select | NP_000017.1:p.Ile403= | |
| NM_001363840.2:c.1209C>A | NP_001350769.1:p.Ile403= | |
| NM_001123378.3:c.1191+532C>A | NP_001116850.1:n.1191+532C>A | |
| NM_001317923.2:c.1017C>A | NP_001304852.1:p.Ile339= | |
| NM_001363840.3:c.1209C>A | NP_001350769.1:p.Ile403= | |
| NR_134256.2:n.1299C>A |