Canonical Allele Identifier: CA497380900

Gene: MC1R

Linked Data

• MyVariant Identifiers: chr16:g.89985828G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89919420G>T , CM000678.2:g.89919420G>T	GRCh38
NC_000016.9:g.89985828G>T , CM000678.1:g.89985828G>T	GRCh37
NC_000016.8:g.88513329G>T	NCBI36
NG_012026.1:g.6542G>T
NG_027810.1:g.2412G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000555147.2:c.162G>T MANE Select	ENSP00000451605.1:p.Val54=
ENST00000639847.1:c.162G>T	ENSP00000492011.1:p.Val54=
ENST00000555147.1:c.162G>T	ENSP00000451605.1:p.Val54=
ENST00000555427.1:c.162G>T	ENSP00000451760.1:p.Val54=
ENST00000556922.1:c.162G>T	ENSP00000451560.1:p.Val54=
NM_002386.3:c.162G>T	NP_002377.4:p.Val54=
NM_002386.4:c.162G>T MANE Select	NP_002377.4:p.Val54=