Canonical Allele Identifier: CA401994995
Gene: MC2R HGNC NCBI

Linked Data

dbSNP Id: rs2045265388

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13884977A>T , CM000680.2:g.13884977A>T GRCh38
NC_000018.9:g.13884976A>T , CM000680.1:g.13884976A>T GRCh37
NC_000018.8:g.13874976A>T NCBI36
NG_011819.1:g.35560T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000327606.4:c.542T>A MANE Select ENSP00000333821.2:p.Leu181Gln
ENST00000327606.3:c.542T>A ENSP00000333821.2:p.Leu181Gln
NM_000529.2:c.542T>A MANE Select NP_000520.1:p.Leu181Gln
NM_001291911.1:c.542T>A NP_001278840.1:p.Leu181Gln
XM_017025781.1:c.542T>A XP_016881270.1:p.Leu181Gln