Canonical Allele Identifier: CA397461531

Gene: MC1R

Linked Data

• ClinVar Variation Id: 2852591
• ClinVar RCV Id: RCV003630909
• MyVariant Identifiers: chr16:g.89986157C>G (hg19) ; chr16:g.89919749C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89919749C>G , CM000678.2:g.89919749C>G	GRCh38
NC_000016.9:g.89986157C>G , CM000678.1:g.89986157C>G	GRCh37
NC_000016.8:g.88513658C>G	NCBI36
NG_012026.1:g.6871C>G
NG_027810.1:g.2741C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555147.2:c.491C>G MANE Select	ENSP00000451605.1:p.Ala164Gly
ENST00000639847.1:c.491C>G	ENSP00000492011.1:p.Ala164Gly
ENST00000555147.1:c.491C>G	ENSP00000451605.1:p.Ala164Gly
ENST00000555427.1:c.491C>G	ENSP00000451760.1:p.Ala164Gly
ENST00000556922.1:c.491C>G	ENSP00000451560.1:p.Ala164Gly
NM_002386.3:c.491C>G	NP_002377.4:p.Ala164Gly
NM_002386.4:c.491C>G MANE Select	NP_002377.4:p.Ala164Gly