Canonical Allele Identifier: CA2641150753
Gene: MC2R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13884592T>G , CM000680.2:g.13884592T>G GRCh38
NC_000018.9:g.13884591T>G , CM000680.1:g.13884591T>G GRCh37
NC_000018.8:g.13874591T>G NCBI36
NG_011819.1:g.35945A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000327606.4:c.*33A>C MANE Select ENSP00000333821.2:n.*33A>C
ENST00000327606.3:c.*33A>C ENSP00000333821.2:n.*33A>C
NM_000529.2:c.*33A>C MANE Select NP_000520.1:n.*33A>C
NM_001291911.1:c.*33A>C NP_001278840.1:n.*33A>C
XM_017025781.1:c.*33A>C XP_016881270.1:n.*33A>C