Canonical Allele Identifier: CA624272367
Gene: MC1R HGNC NCBI

Linked Data

dbSNP Id: rs1272952732
gnomAD v2: 16-89982411-A-G
gnomAD v3: 16-89916003-A-G
gnomAD v4: 16-89916003-A-G
MyVariant Identifiers: chr16:g.89982411A>G (hg19) chr16:g.89916003A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89916003A>G , CM000678.2:g.89916003A>G GRCh38
NC_000016.9:g.89982411A>G , CM000678.1:g.89982411A>G GRCh37
NC_000016.8:g.88509912A>G NCBI36
NG_012026.1:g.3125A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000639847.1:c.-581+863A>G ENSP00000492011.1:n.-581+863A>G
ENST00000555427.1:c.-581+863A>G ENSP00000451760.1:n.-581+863A>G
XR_933899.1:n.2020A>G
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