Canonical Allele Identifier: CA397462863
Gene: MC1R HGNC NCBI

Linked Data

ClinVar Variation Id: 887987
ClinVar RCV Id: RCV001121053
dbSNP Id: rs1264795610
gnomAD v3: 16-89919965-G-A
gnomAD v4: 16-89919965-G-A
MyVariant Identifiers: chr16:g.89986373G>A (hg19) chr16:g.89919965G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89919965G>A , CM000678.2:g.89919965G>A GRCh38
NC_000016.9:g.89986373G>A , CM000678.1:g.89986373G>A GRCh37
NC_000016.8:g.88513874G>A NCBI36
NG_012026.1:g.7087G>A
NG_027810.1:g.2957G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000555147.2:c.707G>A MANE Select ENSP00000451605.1:p.Gly236Asp
ENST00000639847.1:c.707G>A ENSP00000492011.1:p.Gly236Asp
ENST00000555147.1:c.707G>A ENSP00000451605.1:p.Gly236Asp
ENST00000555427.1:c.707G>A ENSP00000451760.1:p.Gly236Asp
ENST00000556922.1:c.707G>A ENSP00000451560.1:p.Gly236Asp
NM_002386.3:c.707G>A NP_002377.4:p.Gly236Asp
NM_002386.4:c.707G>A MANE Select NP_002377.4:p.Gly236Asp
Search 100 bp 5'
Search 100 bp 3'