Canonical Allele Identifier: CA2574042466

Gene: HMGCS2

Linked Data

• gnomAD v4: 1-119759779-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119759779G>T , CM000663.2:g.119759779G>T	GRCh38
NC_000001.10:g.120302402G>T , CM000663.1:g.120302402G>T	GRCh37
NC_000001.9:g.120103925G>T	NCBI36
NG_013348.1:g.14154C>A , LRG_447:g.14154C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369406.8:c.685+85C>A MANE Select	ENSP00000358414.3:n.685+85C>A
ENST00000369406.7:c.685+85C>A	ENSP00000358414.3:n.685+85C>A
ENST00000476640.1:n.581+85C>A
ENST00000544913.2:c.560-497C>A	ENSP00000439495.2:n.560-497C>A
NM_001166107.1:c.560-497C>A , LRG_447t2:c.560-497C>A	NP_001159579.1:n.560-497C>A
NM_005518.3:c.685+85C>A , LRG_447t1:c.685+85C>A	NP_005509.1:n.685+85C>A
XM_011541313.1:c.685+85C>A	XP_011539615.1:n.685+85C>A
XM_011541313.2:c.685+85C>A	XP_011539615.1:n.685+85C>A
NM_005518.4:c.685+85C>A MANE Select	NP_005509.1:n.685+85C>A