Canonical Allele Identifier: CA919934279
Gene: MC2R HGNC NCBI

Linked Data

dbSNP Id: rs1567895375

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13884727del , CM000680.2:g.13884727del GRCh38
NC_000018.9:g.13884726del , CM000680.1:g.13884726del GRCh37
NC_000018.8:g.13874726del NCBI36
NG_011819.1:g.35810del

Transcript Alleles

HGVS Amino-acid Change
ENST00000327606.4:c.792del MANE Select ENSP00000333821.2:p.Ile265SerfsTer26
ENST00000327606.3:c.792del ENSP00000333821.2:p.Ile265SerfsTer26
NM_000529.2:c.792del MANE Select NP_000520.1:p.Ile265SerfsTer26
NM_001291911.1:c.792del NP_001278840.1:p.Ile265SerfsTer26
XM_017025781.1:c.792del XP_016881270.1:p.Ile265SerfsTer26