Canonical Allele Identifier: CA8255635
Gene: MC1R HGNC NCBI

Linked Data

ClinVar Variation Id: 953320
ClinVar RCV Id: RCV001225592
dbSNP Id: rs373224783
ExAC: 16:89986178 C / A
gnomAD v2: 16-89986178-C-A
gnomAD v3: 16-89919770-C-A
gnomAD v4: 16-89919770-C-A
MyVariant Identifiers: chr16:g.89986178C>A (hg19) chr16:g.89919770C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89919770C>A , CM000678.2:g.89919770C>A GRCh38
NC_000016.9:g.89986178C>A , CM000678.1:g.89986178C>A GRCh37
NC_000016.8:g.88513679C>A NCBI36
NG_012026.1:g.6892C>A
NG_027810.1:g.2762C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000555147.2:c.512C>A MANE Select ENSP00000451605.1:p.Ala171Asp
ENST00000639847.1:c.512C>A ENSP00000492011.1:p.Ala171Asp
ENST00000555147.1:c.512C>A ENSP00000451605.1:p.Ala171Asp
ENST00000555427.1:c.512C>A ENSP00000451760.1:p.Ala171Asp
ENST00000556922.1:c.512C>A ENSP00000451560.1:p.Ala171Asp
NM_002386.3:c.512C>A NP_002377.4:p.Ala171Asp
NM_002386.4:c.512C>A MANE Select NP_002377.4:p.Ala171Asp
Search 100 bp 5'
Search 100 bp 3'