Canonical Allele Identifier: CA120921928
Gene: HMGCR HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs17238540

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.75359673T>G , CM000667.2:g.75359673T>G GRCh38
NC_000005.9:g.74655498T>G , CM000667.1:g.74655498T>G GRCh37
NC_000005.8:g.74691254T>G NCBI36
NG_011449.1:g.27506T>G

Transcript Alleles

HGVS Amino-acid change
NM_000859.2:c.2457+117T>G VV NP_000850.1:p.=
NM_001130996.1:c.2298+117T>G VV NP_001124468.1:p.=
XM_011543357.1:c.2517+117T>G XP_011541659.1:p.=
XM_011543358.1:c.2457+117T>G XP_011541660.1:p.=
XM_011543359.1:c.2358+117T>G XP_011541661.1:p.=
NM_001364187.1:c.2457+117T>G VV NP_001351116.1:p.=
NM_000859.3:c.2457+117T>G VV MANE Preferred NP_000850.1:p.=
ENST00000287936.8:c.2457+117T>G ENSP00000287936.4:p.=
ENST00000343975.9:c.2298+117T>G ENSP00000340816.5:p.=
ENST00000509085.5:n.288-312T>G
ENST00000511206.5:c.2457+117T>G ENSP00000426745.1:p.=
ENST00000511986.1:n.139-312T>G ENSP00000420871.1:p.=
ENST00000514315.2:n.515T>G