Canonical Allele Identifier: CA296828539
Gene: MC2R HGNC NCBI

Linked Data

dbSNP Id: rs758727564
COSMIC: COSM71588

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13884684G>A , CM000680.2:g.13884684G>A GRCh38
NC_000018.9:g.13884683G>A , CM000680.1:g.13884683G>A GRCh37
NC_000018.8:g.13874683G>A NCBI36
NG_011819.1:g.35853C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000327606.4:c.835C>T MANE Select ENSP00000333821.2:p.Arg279Trp
ENST00000327606.3:c.835C>T ENSP00000333821.2:p.Arg279Trp
NM_000529.2:c.835C>T MANE Select NP_000520.1:p.Arg279Trp
NM_001291911.1:c.835C>T NP_001278840.1:p.Arg279Trp
XM_017025781.1:c.835C>T XP_016881270.1:p.Arg279Trp