Canonical Allele Identifier: CA8902513
Gene: MC2R HGNC NCBI

Linked Data

dbSNP Id: rs750855000

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13885213G>A , CM000680.2:g.13885213G>A GRCh38
NC_000018.9:g.13885212G>A , CM000680.1:g.13885212G>A GRCh37
NC_000018.8:g.13875212G>A NCBI36
NG_011819.1:g.35324C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000327606.4:c.306C>T MANE Select ENSP00000333821.2:p.Ala102=
ENST00000327606.3:c.306C>T ENSP00000333821.2:p.Ala102=
ENST00000399821.2:c.306C>T ENSP00000382718.2:p.Ala102=
NM_000529.2:c.306C>T MANE Select NP_000520.1:p.Ala102=
NM_001291911.1:c.306C>T NP_001278840.1:p.Ala102=
XM_017025781.1:c.306C>T XP_016881270.1:p.Ala102=