Canonical Allele Identifier: CA397460166

Gene: MC1R

Linked Data

• dbSNP Id: rs1455676637
• gnomAD v2: 16-89985938-A-G
• gnomAD v4: 16-89919530-A-G
• MyVariant Identifiers: chr16:g.89985938A>G (hg19) ; chr16:g.89919530A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89919530A>G , CM000678.2:g.89919530A>G	GRCh38
NC_000016.9:g.89985938A>G , CM000678.1:g.89985938A>G	GRCh37
NC_000016.8:g.88513439A>G	NCBI36
NG_012026.1:g.6652A>G
NG_027810.1:g.2522A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555147.2:c.272A>G MANE Select	ENSP00000451605.1:p.Asn91Ser
ENST00000639847.1:c.272A>G	ENSP00000492011.1:p.Asn91Ser
ENST00000555147.1:c.272A>G	ENSP00000451605.1:p.Asn91Ser
ENST00000555427.1:c.272A>G	ENSP00000451760.1:p.Asn91Ser
ENST00000556922.1:c.272A>G	ENSP00000451560.1:p.Asn91Ser
NM_002386.3:c.272A>G	NP_002377.4:p.Asn91Ser
NM_002386.4:c.272A>G MANE Select	NP_002377.4:p.Asn91Ser