Linked Data
dbSNP Id:
rs1453161331
gnomAD v4:
22-42126505-C-T
MyVariant Identifiers:
chr22:g.42126505C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.42126505C>T , CM000684.2:g.42126505C>T | GRCh38 |
| NC_000022.10:g.42522507C>T , CM000684.1:g.42522507C>T | GRCh37 |
| NC_000022.9:g.40852451C>T | NCBI36 |
| NG_008376.3:g.8487G>A | |
| NG_008376.4:g.9306G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360124.10:c.1361G>A | ENSP00000353241.6:n.1361G>A | |
| ENST00000645361.2:c.*69G>A MANE Select | ENSP00000496150.1:n.*69G>A | |
| ENST00000360124.9:c.1181G>A | ENSP00000353241.5:n.1181G>A | |
| ENST00000360608.9:c.*69G>A | ENSP00000353820.5:n.*69G>A | |
| ENST00000389970.7:c.*69G>A | ENSP00000374620.4:n.*69G>A | |
| NM_000106.5:c.*69G>A | NP_000097.3:n.*69G>A | |
| NM_001025161.2:c.*69G>A | NP_001020332.2:n.*69G>A | |
| XM_011529966.1:c.1452+111G>A | XP_011528268.1:n.1452+111G>A | |
| XM_011529967.1:c.1452+111G>A | XP_011528269.1:n.1452+111G>A | |
| XM_011529968.1:c.1452+111G>A | XP_011528270.1:n.1452+111G>A | |
| XM_011529969.1:c.1308+111G>A | XP_011528271.1:n.1308+111G>A | |
| XM_011529970.1:c.1299+111G>A | XP_011528272.1:n.1299+111G>A | |
| XM_011529971.1:c.*69G>A | XP_011528273.1:n.*69G>A | |
| NM_000106.6:c.*69G>A MANE Select | NP_000097.3:n.*69G>A | |
| NM_001025161.3:c.*69G>A | NP_001020332.2:n.*69G>A |