Canonical Allele Identifier: CA397459298
Gene: MC1R HGNC NCBI

Linked Data

ClinVar Variation Id: 851325
ClinVar RCV Id: RCV001055701
dbSNP Id: rs1215465340
gnomAD v2: 16-89985764-C-T
gnomAD v4: 16-89919356-C-T
MyVariant Identifiers: chr16:g.89985764C>T (hg19) chr16:g.89919356C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89919356C>T , CM000678.2:g.89919356C>T GRCh38
NC_000016.9:g.89985764C>T , CM000678.1:g.89985764C>T GRCh37
NC_000016.8:g.88513265C>T NCBI36
NG_012026.1:g.6478C>T
NG_027810.1:g.2348C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000555147.2:c.98C>T MANE Select ENSP00000451605.1:p.Ala33Val
ENST00000639847.1:c.98C>T ENSP00000492011.1:p.Ala33Val
ENST00000555147.1:c.98C>T ENSP00000451605.1:p.Ala33Val
ENST00000555427.1:c.98C>T ENSP00000451760.1:p.Ala33Val
ENST00000556922.1:c.98C>T ENSP00000451560.1:p.Ala33Val
NM_002386.3:c.98C>T NP_002377.4:p.Ala33Val
NM_002386.4:c.98C>T MANE Select NP_002377.4:p.Ala33Val
Search 100 bp 5'
Search 100 bp 3'