Canonical Allele Identifier: CA2285919394
Gene: MC2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13885042C= , CM000680.2:g.13885042C= GRCh38
NC_000018.9:g.13885041C= , CM000680.1:g.13885041C= GRCh37
NC_000018.8:g.13875041C= NCBI36
NG_011819.1:g.35495G=

Transcript Alleles

HGVS Amino-acid change
ENST00000327606.4:c.477G= MANE Select ENSP00000333821.2:p.Thr159=
ENST00000327606.3:c.477G= ENSP00000333821.2:p.Thr159=
NM_000529.2:c.477G= MANE Select NP_000520.1:p.Thr159=
NM_001291911.1:c.477G= NP_001278840.1:p.Thr159=
XM_017025781.1:c.477G= XP_016881270.1:p.Thr159=