Canonical Allele Identifier: CA2641150739
Gene: MC2R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13884559A>T , CM000680.2:g.13884559A>T GRCh38
NC_000018.9:g.13884558A>T , CM000680.1:g.13884558A>T GRCh37
NC_000018.8:g.13874558A>T NCBI36
NG_011819.1:g.35978T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000327606.4:c.*66T>A MANE Select ENSP00000333821.2:n.*66T>A
ENST00000327606.3:c.*66T>A ENSP00000333821.2:n.*66T>A
NM_000529.2:c.*66T>A MANE Select NP_000520.1:n.*66T>A
NM_001291911.1:c.*66T>A NP_001278840.1:n.*66T>A
XM_017025781.1:c.*66T>A XP_016881270.1:n.*66T>A