Canonical Allele Identifier: CA886268061

Gene: HMGCS2

Linked Data

• ClinVar Variation Id: 2983223
• ClinVar RCV Id: RCV003847838
• dbSNP Id: rs1192655554
• MyVariant Identifiers: chr1:g.120302625A>G (hg19) ; chr1:g.119760002A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119760002A>G , CM000663.2:g.119760002A>G	GRCh38
NC_000001.10:g.120302625A>G , CM000663.1:g.120302625A>G	GRCh37
NC_000001.9:g.120104148A>G	NCBI36
NG_013348.1:g.13931T>C , LRG_447:g.13931T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369406.8:c.560-13T>C MANE Select	ENSP00000358414.3:n.560-13T>C
ENST00000369406.7:c.560-13T>C	ENSP00000358414.3:n.560-13T>C
ENST00000476640.1:n.456-13T>C
ENST00000544913.2:c.560-720T>C	ENSP00000439495.2:n.560-720T>C
NM_001166107.1:c.560-720T>C , LRG_447t2:c.560-720T>C	NP_001159579.1:n.560-720T>C
NM_005518.3:c.560-13T>C , LRG_447t1:c.560-13T>C	NP_005509.1:n.560-13T>C
XM_011541313.1:c.560-13T>C	XP_011539615.1:n.560-13T>C
XM_011541313.2:c.560-13T>C	XP_011539615.1:n.560-13T>C
NM_005518.4:c.560-13T>C MANE Select	NP_005509.1:n.560-13T>C