Canonical Allele Identifier: CA10644651
Gene: MC1R HGNC NCBI

Linked Data

ClinVar Variation Id: 321386
ClinVar RCV Id: RCV000290718
dbSNP Id: rs866287374

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89918050C>T , CM000678.2:g.89918050C>T GRCh38
NC_000016.9:g.89984458C>T , CM000678.1:g.89984458C>T GRCh37
NC_000016.8:g.88511959C>T NCBI36
NG_012026.1:g.5172C>T
NG_027810.1:g.1042C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000639847.1:c.-409+3C>T ENSP00000492011.1:n.-409+3C>T
ENST00000555147.1:c.-1209C>T ENSP00000451605.1:n.-1209C>T
ENST00000555427.1:c.-409+3C>T ENSP00000451760.1:n.-409+3C>T
NM_002386.3:c.-1209C>T NP_002377.4:n.-1209C>T