Canonical Allele Identifier: CA30272912

Gene: HMGCS2

Linked Data

• dbSNP Id: rs1039860218
• gnomAD v4: 1-119760020-C-A
• MyVariant Identifiers: chr1:g.120302643C>A (hg19) ; chr1:g.119760020C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119760020C>A , CM000663.2:g.119760020C>A	GRCh38
NC_000001.10:g.120302643C>A , CM000663.1:g.120302643C>A	GRCh37
NC_000001.9:g.120104166C>A	NCBI36
NG_013348.1:g.13913G>T , LRG_447:g.13913G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369406.8:c.560-31G>T MANE Select	ENSP00000358414.3:n.560-31G>T
ENST00000369406.7:c.560-31G>T	ENSP00000358414.3:n.560-31G>T
ENST00000476640.1:n.456-31G>T
ENST00000544913.2:c.560-738G>T	ENSP00000439495.2:n.560-738G>T
NM_001166107.1:c.560-738G>T , LRG_447t2:c.560-738G>T	NP_001159579.1:n.560-738G>T
NM_005518.3:c.560-31G>T , LRG_447t1:c.560-31G>T	NP_005509.1:n.560-31G>T
XM_011541313.1:c.560-31G>T	XP_011539615.1:n.560-31G>T
XM_011541313.2:c.560-31G>T	XP_011539615.1:n.560-31G>T
NM_005518.4:c.560-31G>T MANE Select	NP_005509.1:n.560-31G>T