Canonical Allele Identifier: CA401994207
Gene: MC2R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13884793C>A , CM000680.2:g.13884793C>A GRCh38
NC_000018.9:g.13884792C>A , CM000680.1:g.13884792C>A GRCh37
NC_000018.8:g.13874792C>A NCBI36
NG_011819.1:g.35744G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000327606.4:c.726G>T MANE Select ENSP00000333821.2:p.Met242Ile
ENST00000327606.3:c.726G>T ENSP00000333821.2:p.Met242Ile
NM_000529.2:c.726G>T MANE Select NP_000520.1:p.Met242Ile
NM_001291911.1:c.726G>T NP_001278840.1:p.Met242Ile
XM_017025781.1:c.726G>T XP_016881270.1:p.Met242Ile