Canonical Allele Identifier: CA401995387
Gene: MC2R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13885149T>A , CM000680.2:g.13885149T>A GRCh38
NC_000018.9:g.13885148T>A , CM000680.1:g.13885148T>A GRCh37
NC_000018.8:g.13875148T>A NCBI36
NG_011819.1:g.35388A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000327606.4:c.370A>T MANE Select ENSP00000333821.2:p.Ile124Phe
ENST00000327606.3:c.370A>T ENSP00000333821.2:p.Ile124Phe
ENST00000399821.2:c.370A>T
NM_000529.2:c.370A>T MANE Select NP_000520.1:p.Ile124Phe
NM_001291911.1:c.370A>T NP_001278840.1:p.Ile124Phe
XM_017025781.1:c.370A>T XP_016881270.1:p.Ile124Phe