Canonical Allele Identifier: CA2574042492
Gene: HMGCS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.119759999G>A , CM000663.2:g.119759999G>A GRCh38
NC_000001.10:g.120302622G>A , CM000663.1:g.120302622G>A GRCh37
NC_000001.9:g.120104145G>A NCBI36
NG_013348.1:g.13934C>T , LRG_447:g.13934C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369406.8:c.560-10C>T MANE Select ENSP00000358414.3:n.560-10C>T
ENST00000369406.7:c.560-10C>T ENSP00000358414.3:n.560-10C>T
ENST00000476640.1:n.456-10C>T
ENST00000544913.2:c.560-717C>T ENSP00000439495.2:n.560-717C>T
NM_001166107.1:c.560-717C>T , LRG_447t2:c.560-717C>T NP_001159579.1:n.560-717C>T
NM_005518.3:c.560-10C>T , LRG_447t1:c.560-10C>T NP_005509.1:n.560-10C>T
XM_011541313.1:c.560-10C>T XP_011539615.1:n.560-10C>T
XM_011541313.2:c.560-10C>T XP_011539615.1:n.560-10C>T
NM_005518.4:c.560-10C>T MANE Select NP_005509.1:n.560-10C>T