Canonical Allele Identifier: CA11933226
Gene: HMGCR HGNC NCBI

Linked Data

dbSNP Id: rs10045497

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
ENST00000287936.9:c.-23-1924C>A MANE Select ENSP00000287936.4:n.-23-1924C>A
ENST00000679456.1:n.122-1924C>A
ENST00000680160.1:c.-23-1924C>A ENSP00000505315.1:n.-23-1924C>A
ENST00000680940.1:c.-53C>A ENSP00000505561.1:n.-53C>A
ENST00000681271.1:c.-23-1924C>A ENSP00000505805.1:n.-23-1924C>A
ENST00000681410.1:c.-23-1924C>A ENSP00000506232.1:n.-23-1924C>A
ENST00000681567.1:c.-23-1924C>A ENSP00000506708.1:n.-23-1924C>A
ENST00000287936.8:c.-23-1924C>A ENSP00000287936.4:n.-23-1924C>A
ENST00000343975.9:c.-23-1924C>A ENSP00000340816.5:n.-23-1924C>A
ENST00000442032.2:c.-24+938C>A ENSP00000409100.2:n.-24+938C>A
ENST00000507942.1:c.-23-1924C>A ENSP00000427340.1:n.-23-1924C>A
ENST00000509431.1:n.56-1924C>A
ENST00000511206.5:c.-23-1924C>A ENSP00000426745.1:n.-23-1924C>A
NM_000859.2:c.-23-1924C>A NP_000850.1:n.-23-1924C>A
NM_001130996.1:c.-23-1924C>A NP_001124468.1:n.-23-1924C>A
XM_011543357.1:c.38-1924C>A XP_011541659.1:n.38-1924C>A
XM_011543358.1:c.-23-1924C>A XP_011541660.1:n.-23-1924C>A
XM_011543359.1:c.38-1924C>A XP_011541661.1:n.38-1924C>A
NM_001364187.1:c.-23-1924C>A NP_001351116.1:n.-23-1924C>A
NM_000859.3:c.-23-1924C>A MANE Select NP_000850.1:n.-23-1924C>A
NM_001130996.2:c.-23-1924C>A NP_001124468.1:n.-23-1924C>A