Canonical Allele Identifier: CA397460696
Gene: MC1R HGNC NCBI

Linked Data

ClinVar Variation Id: 2176995
ClinVar RCV Id: RCV002585312
dbSNP Id: rs1434063620

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89919680A>T , CM000678.2:g.89919680A>T GRCh38
NC_000016.9:g.89986088A>T , CM000678.1:g.89986088A>T GRCh37
NC_000016.8:g.88513589A>T NCBI36
NG_012026.1:g.6802A>T
NG_027810.1:g.2672A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000555147.2:c.422A>T MANE Select ENSP00000451605.1:p.Asp141Val
ENST00000639847.1:c.422A>T ENSP00000492011.1:p.Asp141Val
ENST00000555147.1:c.422A>T ENSP00000451605.1:p.Asp141Val
ENST00000555427.1:c.422A>T ENSP00000451760.1:p.Asp141Val
ENST00000556922.1:c.422A>T ENSP00000451560.1:p.Asp141Val
NM_002386.3:c.422A>T NP_002377.4:p.Asp141Val
NM_002386.4:c.422A>T MANE Select NP_002377.4:p.Asp141Val