Canonical Allele Identifier: CA341858013

Gene: HMGCS2

Linked Data

• MyVariant Identifiers: chr1:g.120295935A>T (hg19) ; chr1:g.119753312A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119753312A>T , CM000663.2:g.119753312A>T	GRCh38
NC_000001.10:g.120295935A>T , CM000663.1:g.120295935A>T	GRCh37
NC_000001.9:g.120097458A>T	NCBI36
NG_013348.1:g.20621T>A , LRG_447:g.20621T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369406.8:c.1262T>A MANE Select	ENSP00000358414.3:p.Phe421Tyr
ENST00000369406.7:c.1262T>A	ENSP00000358414.3:p.Phe421Tyr
ENST00000544913.2:c.1136T>A	ENSP00000439495.2:p.Phe379Tyr
NM_001166107.1:c.1136T>A , LRG_447t2:c.1136T>A	NP_001159579.1:p.Phe379Tyr
NM_005518.3:c.1262T>A , LRG_447t1:c.1262T>A	NP_005509.1:p.Phe421Tyr
XM_011541313.1:c.1097T>A	XP_011539615.1:p.Phe366Tyr
XM_011541313.2:c.1097T>A	XP_011539615.1:p.Phe366Tyr
NM_005518.4:c.1262T>A MANE Select	NP_005509.1:p.Phe421Tyr