Canonical Allele Identifier: CA2285919440
Gene: MC2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13885140C= , CM000680.2:g.13885140C= GRCh38
NC_000018.9:g.13885139C= , CM000680.1:g.13885139C= GRCh37
NC_000018.8:g.13875139C= NCBI36
NG_011819.1:g.35397G=

Transcript Alleles

HGVS Amino-acid change
ENST00000327606.4:c.379G= MANE Select ENSP00000333821.2:p.Asp127=
ENST00000327606.3:c.379G= ENSP00000333821.2:p.Asp127=
NM_000529.2:c.379G= MANE Select NP_000520.1:p.Asp127=
NM_001291911.1:c.379G= NP_001278840.1:p.Asp127=
XM_017025781.1:c.379G= XP_016881270.1:p.Asp127=