Canonical Allele Identifier: CA30272642

Gene: HMGCS2

Linked Data

• dbSNP Id: rs965721644
• gnomAD v3: 1-119759563-T-G
• gnomAD v4: 1-119759563-T-G
• MyVariant Identifiers: chr1:g.119759563T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119759563T>G , CM000663.2:g.119759563T>G	GRCh38
NC_000001.10:g.120302186T>G , CM000663.1:g.120302186T>G	GRCh37
NC_000001.9:g.120103709T>G	NCBI36
NG_013348.1:g.14370A>C , LRG_447:g.14370A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369406.8:c.686-281A>C MANE Select	ENSP00000358414.3:n.686-281A>C
ENST00000369406.7:c.686-281A>C	ENSP00000358414.3:n.686-281A>C
ENST00000476640.1:n.581+301A>C
ENST00000544913.2:c.560-281A>C	ENSP00000439495.2:n.560-281A>C
NM_001166107.1:c.560-281A>C , LRG_447t2:c.560-281A>C	NP_001159579.1:n.560-281A>C
NM_005518.3:c.686-281A>C , LRG_447t1:c.686-281A>C	NP_005509.1:n.686-281A>C
XM_011541313.1:c.685+301A>C	XP_011539615.1:n.685+301A>C
XM_011541313.2:c.685+301A>C	XP_011539615.1:n.685+301A>C
NM_005518.4:c.686-281A>C MANE Select	NP_005509.1:n.686-281A>C