Canonical Allele Identifier: CA2285919248
Gene: MC2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13884735C= , CM000680.2:g.13884735C= GRCh38
NC_000018.9:g.13884734C= , CM000680.1:g.13884734C= GRCh37
NC_000018.8:g.13874734C= NCBI36
NG_011819.1:g.35802G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327606.4:c.784G= MANE Select ENSP00000333821.2:p.Gly262=
ENST00000327606.3:c.784G= ENSP00000333821.2:p.Gly262=
NM_000529.2:c.784G= MANE Select NP_000520.1:p.Gly262=
NM_001291911.1:c.784G= NP_001278840.1:p.Gly262=
XM_017025781.1:c.784G= XP_016881270.1:p.Gly262=