Canonical Allele Identifier: CA776351290
Gene: MC2R HGNC NCBI

Linked Data

dbSNP Id: rs1432496495

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13884932_13884933del , CM000680.2:g.13884932_13884933del GRCh38
NC_000018.9:g.13884931_13884932del , CM000680.1:g.13884931_13884932del GRCh37
NC_000018.8:g.13874931_13874932del NCBI36
NG_011819.1:g.35604_35605del

Transcript Alleles

HGVS Amino-acid Change
ENST00000327606.4:c.586_587del MANE Select ENSP00000333821.2:p.Met196ValfsTer?
ENST00000327606.3:c.586_587del ENSP00000333821.2:p.Met196ValfsTer?
NM_000529.2:c.586_587del MANE Select NP_000520.1:p.Met196ValfsTer?
NM_001291911.1:c.586_587del NP_001278840.1:p.Met196ValfsTer?
XM_017025781.1:c.586_587del XP_016881270.1:p.Met196ValfsTer?