Canonical Allele Identifier: CA341858015

Gene: HMGCS2

Linked Data

• MyVariant Identifiers: chr1:g.120295936A>C (hg19) ; chr1:g.119753313A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119753313A>C , CM000663.2:g.119753313A>C	GRCh38
NC_000001.10:g.120295936A>C , CM000663.1:g.120295936A>C	GRCh37
NC_000001.9:g.120097459A>C	NCBI36
NG_013348.1:g.20620T>G , LRG_447:g.20620T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369406.8:c.1261T>G MANE Select	ENSP00000358414.3:p.Phe421Val
ENST00000369406.7:c.1261T>G	ENSP00000358414.3:p.Phe421Val
ENST00000544913.2:c.1135T>G	ENSP00000439495.2:p.Phe379Val
NM_001166107.1:c.1135T>G , LRG_447t2:c.1135T>G	NP_001159579.1:p.Phe379Val
NM_005518.3:c.1261T>G , LRG_447t1:c.1261T>G	NP_005509.1:p.Phe421Val
XM_011541313.1:c.1096T>G	XP_011539615.1:p.Phe366Val
XM_011541313.2:c.1096T>G	XP_011539615.1:p.Phe366Val
NM_005518.4:c.1261T>G MANE Select	NP_005509.1:p.Phe421Val