Canonical Allele Identifier: CA397460168
Gene: MC1R HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.89985938A>C (hg19) chr16:g.89919530A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89919530A>C , CM000678.2:g.89919530A>C GRCh38
NC_000016.9:g.89985938A>C , CM000678.1:g.89985938A>C GRCh37
NC_000016.8:g.88513439A>C NCBI36
NG_012026.1:g.6652A>C
NG_027810.1:g.2522A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000555147.2:c.272A>C MANE Select ENSP00000451605.1:p.Asn91Thr
ENST00000639847.1:c.272A>C ENSP00000492011.1:p.Asn91Thr
ENST00000555147.1:c.272A>C ENSP00000451605.1:p.Asn91Thr
ENST00000555427.1:c.272A>C ENSP00000451760.1:p.Asn91Thr
ENST00000556922.1:c.272A>C ENSP00000451560.1:p.Asn91Thr
NM_002386.3:c.272A>C NP_002377.4:p.Asn91Thr
NM_002386.4:c.272A>C MANE Select NP_002377.4:p.Asn91Thr
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