Canonical Allele Identifier: CA401993541
Gene: MC2R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13884641C>G , CM000680.2:g.13884641C>G GRCh38
NC_000018.9:g.13884640C>G , CM000680.1:g.13884640C>G GRCh37
NC_000018.8:g.13874640C>G NCBI36
NG_011819.1:g.35896G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000327606.4:c.878G>C MANE Select ENSP00000333821.2:p.Cys293Ser
ENST00000327606.3:c.878G>C ENSP00000333821.2:p.Cys293Ser
NM_000529.2:c.878G>C MANE Select NP_000520.1:p.Cys293Ser
NM_001291911.1:c.878G>C NP_001278840.1:p.Cys293Ser
XM_017025781.1:c.878G>C XP_016881270.1:p.Cys293Ser