Canonical Allele Identifier: CA397460883
Gene: MC1R HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.89986124A>C (hg19) chr16:g.89919716A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89919716A>C , CM000678.2:g.89919716A>C GRCh38
NC_000016.9:g.89986124A>C , CM000678.1:g.89986124A>C GRCh37
NC_000016.8:g.88513625A>C NCBI36
NG_012026.1:g.6838A>C
NG_027810.1:g.2708A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000555147.2:c.458A>C MANE Select ENSP00000451605.1:p.His153Pro
ENST00000639847.1:c.458A>C ENSP00000492011.1:p.His153Pro
ENST00000555147.1:c.458A>C ENSP00000451605.1:p.His153Pro
ENST00000555427.1:c.458A>C ENSP00000451760.1:p.His153Pro
ENST00000556922.1:c.458A>C ENSP00000451560.1:p.His153Pro
NM_002386.3:c.458A>C NP_002377.4:p.His153Pro
NM_002386.4:c.458A>C MANE Select NP_002377.4:p.His153Pro
Search 100 bp 5'
Search 100 bp 3'