Canonical Allele Identifier: CA8255634
Gene: MC1R HGNC NCBI

Linked Data

ClinVar Variation Id: 548659
dbSNP Id: rs373224783

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89919770C>G , CM000678.2:g.89919770C>G GRCh38
NC_000016.9:g.89986178C>G , CM000678.1:g.89986178C>G GRCh37
NC_000016.8:g.88513679C>G NCBI36
NG_012026.1:g.6892C>G
NG_027810.1:g.2762C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000555147.2:c.512C>G MANE Select ENSP00000451605.1:p.Ala171Gly
ENST00000639847.1:c.512C>G ENSP00000492011.1:p.Ala171Gly
ENST00000555147.1:c.512C>G ENSP00000451605.1:p.Ala171Gly
ENST00000555427.1:c.512C>G ENSP00000451760.1:p.Ala171Gly
ENST00000556922.1:c.512C>G ENSP00000451560.1:p.Ala171Gly
NM_002386.3:c.512C>G NP_002377.4:p.Ala171Gly
NM_002386.4:c.512C>G MANE Select NP_002377.4:p.Ala171Gly