Canonical Allele Identifier: CA2641150743
Gene: MC2R HGNC NCBI

Linked Data

dbSNP Id: rs2149134758

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13884569del , CM000680.2:g.13884569del GRCh38
NC_000018.9:g.13884568del , CM000680.1:g.13884568del GRCh37
NC_000018.8:g.13874568del NCBI36
NG_011819.1:g.35968del

Transcript Alleles

HGVS Amino-acid change
ENST00000327606.4:c.*56del MANE Select ENSP00000333821.2:n.*56del
ENST00000327606.3:c.*56del ENSP00000333821.2:n.*56del
NM_000529.2:c.*56del MANE Select NP_000520.1:n.*56del
NM_001291911.1:c.*56del NP_001278840.1:n.*56del
XM_017025781.1:c.*56del XP_016881270.1:n.*56del