Canonical Allele Identifier: CA503010662
Gene: MC2R HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.13884660T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13884661T>A , CM000680.2:g.13884661T>A GRCh38
NC_000018.9:g.13884660T>A , CM000680.1:g.13884660T>A GRCh37
NC_000018.8:g.13874660T>A NCBI36
NG_011819.1:g.35876A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000327606.4:c.858A>T MANE Select ENSP00000333821.2:p.Ala286=
ENST00000327606.3:c.858A>T ENSP00000333821.2:p.Ala286=
NM_000529.2:c.858A>T MANE Select NP_000520.1:p.Ala286=
NM_001291911.1:c.858A>T NP_001278840.1:p.Ala286=
XM_017025781.1:c.858A>T XP_016881270.1:p.Ala286=