Canonical Allele Identifier: CA2242009590
Gene: MC1R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89919752T= , CM000678.2:g.89919752T= GRCh38
NC_000016.9:g.89986160T= , CM000678.1:g.89986160T= GRCh37
NC_000016.8:g.88513661T= NCBI36
NG_012026.1:g.6874T=
NG_027810.1:g.2744T=

Transcript Alleles

HGVS Amino-acid change
ENST00000555147.2:c.494T= MANE Select ENSP00000451605.1:p.Val165=
ENST00000639847.1:c.494T= ENSP00000492011.1:p.Val165=
ENST00000555147.1:c.494T= ENSP00000451605.1:p.Val165=
ENST00000555427.1:c.494T= ENSP00000451760.1:p.Val165=
ENST00000556922.1:c.494T= ENSP00000451560.1:p.Val165=
NM_002386.3:c.494T= NP_002377.4:p.Val165=
NM_002386.4:c.494T= MANE Select NP_002377.4:p.Val165=