Canonical Allele Identifier: CA11933226

Gene: HMGCR

Identifiers and link-outs to other resources

• dbSNP Id: rs10045497
• gnomAD: 5:74636484 C / A
• MyVariant Identifiers: chr5:g.74636484C>A (hg19) ; chr5:g.75340659C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.75340659C>A , CM000667.2:g.75340659C>A	GRCh38
NC_000005.9:g.74636484C>A , CM000667.1:g.74636484C>A	GRCh37
NC_000005.8:g.74672240C>A	NCBI36
NG_011449.1:g.8492C>A

Transcript Alleles

HGVS	Amino-acid change
NM_000859.2:c.-23-1924C>A VV	NP_000850.1:p.=
NM_001130996.1:c.-23-1924C>A VV	NP_001124468.1:p.=
XM_011543357.1:c.38-1924C>A	XP_011541659.1:p.=
XM_011543358.1:c.-23-1924C>A	XP_011541660.1:p.=
XM_011543359.1:c.38-1924C>A	XP_011541661.1:p.=
NM_001364187.1:c.-23-1924C>A VV	NP_001351116.1:p.=
NM_000859.3:c.-23-1924C>A VV MANE Preferred	NP_000850.1:p.=
ENST00000287936.8:c.-23-1924C>A	ENSP00000287936.4:p.=
ENST00000343975.9:c.-23-1924C>A	ENSP00000340816.5:p.=
ENST00000442032.2:c.-24+938C>A	ENSP00000409100.2:p.=
ENST00000507942.1:c.-23-1924C>A	ENSP00000427340.1:p.=
ENST00000509431.1:n.56-1924C>A
ENST00000511206.5:c.-23-1924C>A	ENSP00000426745.1:p.=