Linked Data
ClinVar Variation Id:
978552
ClinVar RCV Id:
RCV001257263
dbSNP Id:
rs1354679314
gnomAD v4:
7-2539801-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.2539801G>A , CM000669.2:g.2539801G>A | GRCh38 |
| NC_000007.13:g.2579435G>A , CM000669.1:g.2579435G>A | GRCh37 |
| NC_000007.12:g.2545961G>A | NCBI36 |
| NG_032167.1:g.20958C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000340611.9:c.1483C>T MANE Select | ENSP00000339637.4:p.Pro495Ser | |
| ENST00000340611.8:c.1483C>T | ENSP00000339637.4:p.Pro495Ser | |
| ENST00000467558.5:n.2855C>T | ||
| ENST00000469750.5:n.4055C>T | ||
| ENST00000473879.1:n.199C>T | ||
| ENST00000493232.5:n.4219C>T | ||
| NM_152743.3:c.1483C>T | NP_689956.2:p.Pro495Ser | |
| XM_005249643.3:c.1483C>T | XP_005249700.1:p.Pro495Ser | |
| XM_011515177.1:c.1567C>T | XP_011513479.1:p.Pro523Ser | |
| XM_011515178.1:c.1567C>T | XP_011513480.1:p.Pro523Ser | |
| XM_011515179.1:c.1564C>T | XP_011513481.1:p.Pro522Ser | |
| XM_011515180.1:c.1537C>T | XP_011513482.1:p.Pro513Ser | |
| XM_011515181.1:c.1567C>T | XP_011513483.1:p.Pro523Ser | |
| XM_011515182.1:c.1567C>T | XP_011513484.1:p.Pro523Ser | |
| XM_011515183.1:c.1042C>T | XP_011513485.1:p.Pro348Ser | |
| XM_011515184.1:c.1042C>T | XP_011513486.1:p.Pro348Ser | |
| XM_011515185.1:c.1483C>T | XP_011513487.1:p.Pro495Ser | |
| XM_011515186.1:c.1567C>T | XP_011513488.1:p.Pro523Ser | |
| XM_011515187.1:c.139C>T | XP_011513489.1:p.Pro47Ser | |
| NM_001350626.1:c.1483C>T | NP_001337555.1:p.Pro495Ser | |
| NM_001350627.1:c.958C>T | NP_001337556.1:p.Pro320Ser | |
| NR_146879.1:n.1900C>T | ||
| XM_011515177.2:c.1567C>T | XP_011513479.1:p.Pro523Ser | |
| XM_011515179.2:c.1564C>T | XP_011513481.1:p.Pro522Ser | |
| XM_011515181.2:c.1567C>T | XP_011513483.1:p.Pro523Ser | |
| XM_011515182.2:c.1567C>T | XP_011513484.1:p.Pro523Ser | |
| XM_011515184.3:c.1042C>T | XP_011513486.1:p.Pro348Ser | |
| XM_011515186.2:c.1567C>T | XP_011513488.1:p.Pro523Ser | |
| XM_017011833.1:c.1480C>T | XP_016867322.1:p.Pro494Ser | |
| XM_017011834.1:c.1480C>T | XP_016867323.1:p.Pro494Ser | |
| XM_017011836.2:c.1483C>T | XP_016867325.1:p.Pro495Ser | |
| XM_024446682.1:c.139C>T | XP_024302450.1:p.Pro47Ser | |
| NM_152743.4:c.1483C>T MANE Select | NP_689956.2:p.Pro495Ser | |
| NM_001350626.2:c.1483C>T | NP_001337555.1:p.Pro495Ser | |
| NM_001350627.2:c.958C>T | NP_001337556.1:p.Pro320Ser | |
| NR_146879.2:n.1666C>T |