Canonical Allele Identifier: CA420026685

Gene: HMGCS2

Linked Data

• MyVariant Identifiers: chr1:g.120302551G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119759928G>T , CM000663.2:g.119759928G>T	GRCh38
NC_000001.10:g.120302551G>T , CM000663.1:g.120302551G>T	GRCh37
NC_000001.9:g.120104074G>T	NCBI36
NG_013348.1:g.14005C>A , LRG_447:g.14005C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369406.8:c.621C>A MANE Select	ENSP00000358414.3:p.Pro207=
ENST00000369406.7:c.621C>A	ENSP00000358414.3:p.Pro207=
ENST00000476640.1:n.517C>A
ENST00000544913.2:c.560-646C>A	ENSP00000439495.2:n.560-646C>A
NM_001166107.1:c.560-646C>A , LRG_447t2:c.560-646C>A	NP_001159579.1:n.560-646C>A
NM_005518.3:c.621C>A , LRG_447t1:c.621C>A	NP_005509.1:p.Pro207=
XM_011541313.1:c.621C>A	XP_011539615.1:p.Pro207=
XM_011541313.2:c.621C>A	XP_011539615.1:p.Pro207=
NM_005518.4:c.621C>A MANE Select	NP_005509.1:p.Pro207=