Linked Data
ClinVar Variation Id:
363299
dbSNP Id:
rs150524359
ExAC:
8:55541005 C / T
gnomAD v2:
8-55541005-C-T
gnomAD v3:
8-54628445-C-T
gnomAD v4:
8-54628445-C-T
COSMIC:
COSM3395359
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.54628445C>T , CM000670.2:g.54628445C>T | GRCh38 |
| NC_000008.10:g.55541005C>T , CM000670.1:g.55541005C>T | GRCh37 |
| NC_000008.9:g.55703558C>T | NCBI36 |
| NG_009840.1:g.17379C>T | |
| NG_009840.2:g.17379C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000220676.2:c.4563C>T MANE Select | ENSP00000220676.1:p.Asn1521= | |
| ENST00000636932.1:c.787+6157C>T | ENSP00000489857.1:n.787+6157C>T | |
| ENST00000637698.1:c.787+6157C>T | ENSP00000490104.1:n.787+6157C>T | |
| ENST00000220676.1:c.4563C>T | ENSP00000220676.1:p.Asn1521= | |
| NM_006269.1:c.4563C>T | NP_006260.1:p.Asn1521= | |
| XM_017013721.1:c.4584C>T | XP_016869210.1:p.Asn1528= | |
| XM_017013722.1:c.4563C>T | XP_016869211.1:p.Asn1521= | |
| NM_001375654.1:c.787+6157C>T | NP_001362583.1:n.787+6157C>T | |
| NM_006269.2:c.4563C>T MANE Select | NP_006260.1:p.Asn1521= |