Canonical Allele Identifier: CA2285919144
Gene: MC2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13884563T= , CM000680.2:g.13884563T= GRCh38
NC_000018.9:g.13884562T= , CM000680.1:g.13884562T= GRCh37
NC_000018.8:g.13874562T= NCBI36
NG_011819.1:g.35974A=

Transcript Alleles

HGVS Amino-acid change
ENST00000327606.4:c.*62A= MANE Select ENSP00000333821.2:n.*62A=
ENST00000327606.3:c.*62A= ENSP00000333821.2:n.*62A=
NM_000529.2:c.*62A= MANE Select NP_000520.1:n.*62A=
NM_001291911.1:c.*62A= NP_001278840.1:n.*62A=
XM_017025781.1:c.*62A= XP_016881270.1:n.*62A=