Linked Data
dbSNP Id:
rs756199344
ExAC:
12:57905623 C / A
gnomAD v2:
12-57905623-C-A
gnomAD v3:
12-57511840-C-A
gnomAD v4:
12-57511840-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57511840C>A , CM000674.2:g.57511840C>A | GRCh38 |
| NC_000012.11:g.57905623C>A , CM000674.1:g.57905623C>A | GRCh37 |
| NC_000012.10:g.56191890C>A | NCBI36 |
| NG_034077.1:g.28888C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262027.10:c.1511C>A MANE Select | ENSP00000262027.5:p.Pro504His | |
| ENST00000262027.9:c.1511C>A | ENSP00000262027.5:p.Pro504His | |
| ENST00000447721.6:n.1153C>A | ||
| ENST00000537638.6:c.1511C>A | ENSP00000446168.2:p.Pro504His | |
| ENST00000545888.6:c.*1012C>A | ENSP00000439307.2:n.*1012C>A | |
| ENST00000546971.5:n.255C>A | ||
| ENST00000548630.1:n.72C>A | ||
| ENST00000548944.1:c.134-4655C>A | ENSP00000449071.1:n.134-4655C>A | |
| ENST00000549048.1:n.44C>A | ||
| ENST00000628866.2:c.*1012C>A | ENSP00000486738.1:n.*1012C>A | |
| NM_004990.3:c.1511C>A | NP_004981.2:p.Pro504His | |
| XM_006719398.2:c.809C>A | XP_006719461.1:p.Pro270His | |
| XM_011538353.1:c.1511C>A | XP_011536655.1:p.Pro504His | |
| XM_006719398.4:c.809C>A | XP_006719461.1:p.Pro270His | |
| XR_001748704.2:n.1534C>A | ||
| XR_002957327.1:n.1458C>A | ||
| NM_004990.4:c.1511C>A MANE Select | NP_004981.2:p.Pro504His |