Canonical Allele Identifier: CA2285919147
Gene: MC2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13884566A= , CM000680.2:g.13884566A= GRCh38
NC_000018.9:g.13884565A= , CM000680.1:g.13884565A= GRCh37
NC_000018.8:g.13874565A= NCBI36
NG_011819.1:g.35971T=

Transcript Alleles

HGVS Amino-acid change
ENST00000327606.4:c.*59T= MANE Select ENSP00000333821.2:n.*59T=
ENST00000327606.3:c.*59T= ENSP00000333821.2:n.*59T=
NM_000529.2:c.*59T= MANE Select NP_000520.1:n.*59T=
NM_001291911.1:c.*59T= NP_001278840.1:n.*59T=
XM_017025781.1:c.*59T= XP_016881270.1:n.*59T=