Canonical Allele Identifier: CA8255640
Gene: MC1R HGNC NCBI

Linked Data

ClinVar Variation Id: 2164142
ClinVar RCV Id: RCV003092695
dbSNP Id: rs776829551

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89919777C>T , CM000678.2:g.89919777C>T GRCh38
NC_000016.9:g.89986185C>T , CM000678.1:g.89986185C>T GRCh37
NC_000016.8:g.88513686C>T NCBI36
NG_012026.1:g.6899C>T
NG_027810.1:g.2769C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000555147.2:c.519C>T MANE Select ENSP00000451605.1:p.Val173=
ENST00000639847.1:c.519C>T ENSP00000492011.1:p.Val173=
ENST00000555147.1:c.519C>T ENSP00000451605.1:p.Val173=
ENST00000555427.1:c.519C>T ENSP00000451760.1:p.Val173=
ENST00000556922.1:c.519C>T ENSP00000451560.1:p.Val173=
NM_002386.3:c.519C>T NP_002377.4:p.Val173=
NM_002386.4:c.519C>T MANE Select NP_002377.4:p.Val173=