Canonical Allele Identifier: CA341858723

Gene: HMGCS2

Linked Data

• MyVariant Identifiers: chr1:g.120298075C>G (hg19) ; chr1:g.119755452C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119755452C>G , CM000663.2:g.119755452C>G	GRCh38
NC_000001.10:g.120298075C>G , CM000663.1:g.120298075C>G	GRCh37
NC_000001.9:g.120099598C>G	NCBI36
NG_013348.1:g.18481G>C , LRG_447:g.18481G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369406.8:c.1162G>C MANE Select	ENSP00000358414.3:p.Gly388Arg
ENST00000369406.7:c.1162G>C	ENSP00000358414.3:p.Gly388Arg
ENST00000472375.5:n.609G>C
ENST00000544913.2:c.1036G>C	ENSP00000439495.2:p.Gly346Arg
NM_001166107.1:c.1036G>C , LRG_447t2:c.1036G>C	NP_001159579.1:p.Gly346Arg
NM_005518.3:c.1162G>C , LRG_447t1:c.1162G>C	NP_005509.1:p.Gly388Arg
XM_011541313.1:c.997G>C	XP_011539615.1:p.Gly333Arg
XM_011541313.2:c.997G>C	XP_011539615.1:p.Gly333Arg
NM_005518.4:c.1162G>C MANE Select	NP_005509.1:p.Gly388Arg