Canonical Allele Identifier: CA397462644
Gene: MC1R HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.89986328T>G (hg19) chr16:g.89919920T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89919920T>G , CM000678.2:g.89919920T>G GRCh38
NC_000016.9:g.89986328T>G , CM000678.1:g.89986328T>G GRCh37
NC_000016.8:g.88513829T>G NCBI36
NG_012026.1:g.7042T>G
NG_027810.1:g.2912T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000555147.2:c.662T>G MANE Select ENSP00000451605.1:p.Ile221Ser
ENST00000639847.1:c.662T>G ENSP00000492011.1:p.Ile221Ser
ENST00000555147.1:c.662T>G ENSP00000451605.1:p.Ile221Ser
ENST00000555427.1:c.662T>G ENSP00000451760.1:p.Ile221Ser
ENST00000556922.1:c.662T>G ENSP00000451560.1:p.Ile221Ser
NM_002386.3:c.662T>G NP_002377.4:p.Ile221Ser
NM_002386.4:c.662T>G MANE Select NP_002377.4:p.Ile221Ser
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