Canonical Allele Identifier: CA988024993
Gene: MC2R HGNC NCBI

Linked Data

dbSNP Id: rs1567895263

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13884587G>A , CM000680.2:g.13884587G>A GRCh38
NC_000018.9:g.13884586G>A , CM000680.1:g.13884586G>A GRCh37
NC_000018.8:g.13874586G>A NCBI36
NG_011819.1:g.35950C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000327606.4:c.*38C>T MANE Select ENSP00000333821.2:n.*38C>T
ENST00000327606.3:c.*38C>T ENSP00000333821.2:n.*38C>T
NM_000529.2:c.*38C>T MANE Select NP_000520.1:n.*38C>T
NM_001291911.1:c.*38C>T NP_001278840.1:n.*38C>T
XM_017025781.1:c.*38C>T XP_016881270.1:n.*38C>T