Canonical Allele Identifier: CA503248160
Gene: MC2R HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.13884819G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13884820G>A , CM000680.2:g.13884820G>A GRCh38
NC_000018.9:g.13884819G>A , CM000680.1:g.13884819G>A GRCh37
NC_000018.8:g.13874819G>A NCBI36
NG_011819.1:g.35717C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000327606.4:c.699C>T MANE Select ENSP00000333821.2:p.Ala233=
ENST00000327606.3:c.699C>T ENSP00000333821.2:p.Ala233=
NM_000529.2:c.699C>T MANE Select NP_000520.1:p.Ala233=
NM_001291911.1:c.699C>T NP_001278840.1:p.Ala233=
XM_017025781.1:c.699C>T XP_016881270.1:p.Ala233=