Canonical Allele Identifier: CA401994071
Gene: MC2R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13884764G>C , CM000680.2:g.13884764G>C GRCh38
NC_000018.9:g.13884763G>C , CM000680.1:g.13884763G>C GRCh37
NC_000018.8:g.13874763G>C NCBI36
NG_011819.1:g.35773C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000327606.3:c.755C>G ENSP00000333821.2:p.Ala252Gly
NM_000529.2:c.755C>G MANE Select NP_000520.1:p.Ala252Gly
NM_001291911.1:c.755C>G NP_001278840.1:p.Ala252Gly
XM_017025781.1:c.755C>G XP_016881270.1:p.Ala252Gly