Canonical Allele Identifier: CA2285919166
Gene: MC2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13884602T= , CM000680.2:g.13884602T= GRCh38
NC_000018.9:g.13884601T= , CM000680.1:g.13884601T= GRCh37
NC_000018.8:g.13874601T= NCBI36
NG_011819.1:g.35935A=

Transcript Alleles

HGVS Amino-acid change
ENST00000327606.4:c.*23A= MANE Select ENSP00000333821.2:n.*23A=
ENST00000327606.3:c.*23A= ENSP00000333821.2:n.*23A=
NM_000529.2:c.*23A= MANE Select NP_000520.1:n.*23A=
NM_001291911.1:c.*23A= NP_001278840.1:n.*23A=
XM_017025781.1:c.*23A= XP_016881270.1:n.*23A=