Canonical Allele Identifier: CA2647398800

Gene: HMGCS2

Linked Data

• gnomAD v4: 1-119753260-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119753260A>T , CM000663.2:g.119753260A>T	GRCh38
NC_000001.10:g.120295883A>T , CM000663.1:g.120295883A>T	GRCh37
NC_000001.9:g.120097406A>T	NCBI36
NG_013348.1:g.20673T>A , LRG_447:g.20673T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369406.8:c.1294+20T>A MANE Select	ENSP00000358414.3:n.1294+20T>A
ENST00000369406.7:c.1294+20T>A	ENSP00000358414.3:n.1294+20T>A
ENST00000544913.2:c.1168+20T>A	ENSP00000439495.2:n.1168+20T>A
NM_001166107.1:c.1168+20T>A , LRG_447t2:c.1168+20T>A	NP_001159579.1:n.1168+20T>A
NM_005518.3:c.1294+20T>A , LRG_447t1:c.1294+20T>A	NP_005509.1:n.1294+20T>A
XM_011541313.1:c.1129+20T>A	XP_011539615.1:n.1129+20T>A
XM_011541313.2:c.1129+20T>A	XP_011539615.1:n.1129+20T>A
NM_005518.4:c.1294+20T>A MANE Select	NP_005509.1:n.1294+20T>A