Canonical Allele Identifier: CA2734686331
Gene: MC2R HGNC NCBI

Linked Data

dbSNP Id: rs2149134749

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13884560T>A , CM000680.2:g.13884560T>A GRCh38
NC_000018.9:g.13884559T>A , CM000680.1:g.13884559T>A GRCh37
NC_000018.8:g.13874559T>A NCBI36
NG_011819.1:g.35977A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000327606.4:c.*65A>T MANE Select ENSP00000333821.2:n.*65A>T
ENST00000327606.3:c.*65A>T ENSP00000333821.2:n.*65A>T
NM_000529.2:c.*65A>T MANE Select NP_000520.1:n.*65A>T
NM_001291911.1:c.*65A>T NP_001278840.1:n.*65A>T
XM_017025781.1:c.*65A>T XP_016881270.1:n.*65A>T