Canonical Allele Identifier: CA2285919393
Gene: MC2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13885041C= , CM000680.2:g.13885041C= GRCh38
NC_000018.9:g.13885040C= , CM000680.1:g.13885040C= GRCh37
NC_000018.8:g.13875040C= NCBI36
NG_011819.1:g.35496G=

Transcript Alleles

HGVS Amino-acid change
ENST00000327606.4:c.478G= MANE Select ENSP00000333821.2:p.Gly160=
ENST00000327606.3:c.478G= ENSP00000333821.2:p.Gly160=
NM_000529.2:c.478G= MANE Select NP_000520.1:p.Gly160=
NM_001291911.1:c.478G= NP_001278840.1:p.Gly160=
XM_017025781.1:c.478G= XP_016881270.1:p.Gly160=