Canonical Allele Identifier: CA2285919205
Gene: MC2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13884658G= , CM000680.2:g.13884658G= GRCh38
NC_000018.9:g.13884657G= , CM000680.1:g.13884657G= GRCh37
NC_000018.8:g.13874657G= NCBI36
NG_011819.1:g.35879C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327606.4:c.861C= MANE Select ENSP00000333821.2:p.Phe287=
ENST00000327606.3:c.861C= ENSP00000333821.2:p.Phe287=
NM_000529.2:c.861C= MANE Select NP_000520.1:p.Phe287=
NM_001291911.1:c.861C= NP_001278840.1:p.Phe287=
XM_017025781.1:c.861C= XP_016881270.1:p.Phe287=