Canonical Allele Identifier: CA2285919177
Gene: MC2R HGNC NCBI

Linked Data

dbSNP Id: rs2045260391

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13884612G>A , CM000680.2:g.13884612G>A GRCh38
NC_000018.9:g.13884611G>A , CM000680.1:g.13884611G>A GRCh37
NC_000018.8:g.13874611G>A NCBI36
NG_011819.1:g.35925C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000327606.4:c.*13C>T MANE Select ENSP00000333821.2:n.*13C>T
ENST00000327606.3:c.*13C>T ENSP00000333821.2:n.*13C>T
NM_000529.2:c.*13C>T MANE Select NP_000520.1:n.*13C>T
NM_001291911.1:c.*13C>T NP_001278840.1:n.*13C>T
XM_017025781.1:c.*13C>T XP_016881270.1:n.*13C>T