Canonical Allele Identifier: CA286607469
Gene: MC1R HGNC NCBI

Linked Data

dbSNP Id: rs1805007

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89919709C>G , CM000678.2:g.89919709C>G GRCh38
NC_000016.9:g.89986117C>G , CM000678.1:g.89986117C>G GRCh37
NC_000016.8:g.88513618C>G NCBI36
NG_012026.1:g.6831C>G
NG_027810.1:g.2701C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000555147.2:c.451C>G MANE Select ENSP00000451605.1:p.Arg151Gly
ENST00000639847.1:c.451C>G ENSP00000492011.1:p.Arg151Gly
ENST00000555147.1:c.451C>G ENSP00000451605.1:p.Arg151Gly
ENST00000555427.1:c.451C>G ENSP00000451760.1:p.Arg151Gly
ENST00000556922.1:c.451C>G ENSP00000451560.1:p.Arg151Gly
NM_002386.3:c.451C>G NP_002377.4:p.Arg151Gly
NM_002386.4:c.451C>G MANE Select NP_002377.4:p.Arg151Gly