Canonical Allele Identifier: CA2285919376
Gene: MC2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13885006A= , CM000680.2:g.13885006A= GRCh38
NC_000018.9:g.13885005A= , CM000680.1:g.13885005A= GRCh37
NC_000018.8:g.13875005A= NCBI36
NG_011819.1:g.35531T=

Transcript Alleles

HGVS Amino-acid change
ENST00000327606.4:c.513T= MANE Select ENSP00000333821.2:p.His171=
ENST00000327606.3:c.513T= ENSP00000333821.2:p.His171=
NM_000529.2:c.513T= MANE Select NP_000520.1:p.His171=
NM_001291911.1:c.513T= NP_001278840.1:p.His171=
XM_017025781.1:c.513T= XP_016881270.1:p.His171=