Canonical Allele Identifier: CA30272668
Gene: HMGCS2 HGNC NCBI

Linked Data

dbSNP Id: rs1038193689
MyVariant Identifiers: chr1:g.120302255C>T (hg19) chr1:g.119759632C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.119759632C>T , CM000663.2:g.119759632C>T GRCh38
NC_000001.10:g.120302255C>T , CM000663.1:g.120302255C>T GRCh37
NC_000001.9:g.120103778C>T NCBI36
NG_013348.1:g.14301G>A , LRG_447:g.14301G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369406.8:c.685+232G>A MANE Select ENSP00000358414.3:n.685+232G>A
ENST00000369406.7:c.685+232G>A ENSP00000358414.3:n.685+232G>A
ENST00000476640.1:n.581+232G>A
ENST00000544913.2:c.560-350G>A ENSP00000439495.2:n.560-350G>A
NM_001166107.1:c.560-350G>A , LRG_447t2:c.560-350G>A NP_001159579.1:n.560-350G>A
NM_005518.3:c.685+232G>A , LRG_447t1:c.685+232G>A NP_005509.1:n.685+232G>A
XM_011541313.1:c.685+232G>A XP_011539615.1:n.685+232G>A
XM_011541313.2:c.685+232G>A XP_011539615.1:n.685+232G>A
NM_005518.4:c.685+232G>A MANE Select NP_005509.1:n.685+232G>A
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