Canonical Allele Identifier: CA2576463995
Gene: MC2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13885545A>T , CM000680.2:g.13885545A>T GRCh38
NC_000018.9:g.13885544A>T , CM000680.1:g.13885544A>T GRCh37
NC_000018.8:g.13875544A>T NCBI36
NG_011819.1:g.34992T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000327606.4:c.-27T>A MANE Select ENSP00000333821.2:n.-27T>A
ENST00000327606.3:c.-27T>A ENSP00000333821.2:n.-27T>A
ENST00000399821.2:c.-27T>A ENSP00000382718.2:n.-27T>A
NM_000529.2:c.-27T>A MANE Select NP_000520.1:n.-27T>A
NM_001291911.1:c.-27T>A NP_001278840.1:n.-27T>A
XM_017025781.1:c.-27T>A XP_016881270.1:n.-27T>A