Canonical Allele Identifier: CA813985665
Gene: HMGCR HGNC NCBI

Linked Data

dbSNP Id: rs1367521646

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.75355291T>G , CM000667.2:g.75355291T>G GRCh38
NC_000005.9:g.74651116T>G , CM000667.1:g.74651116T>G GRCh37
NC_000005.8:g.74686872T>G NCBI36
NG_011449.1:g.23124T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000287936.9:c.1723-74T>G MANE Select ENSP00000287936.4:n.1723-74T>G
ENST00000679456.1:n.2560-74T>G
ENST00000680160.1:c.1723-74T>G ENSP00000505315.1:n.1723-74T>G
ENST00000680940.1:c.1723-74T>G ENSP00000505561.1:n.1723-74T>G
ENST00000681271.1:c.1723-74T>G ENSP00000505805.1:n.1723-74T>G
ENST00000681410.1:c.1723-74T>G ENSP00000506232.1:n.1723-74T>G
ENST00000681567.1:c.*2272-74T>G ENSP00000506708.1:n.*2272-74T>G
ENST00000287936.8:c.1723-74T>G ENSP00000287936.4:n.1723-74T>G
ENST00000343975.9:c.1564-74T>G ENSP00000340816.5:n.1564-74T>G
ENST00000508070.1:n.112T>G
ENST00000511206.5:c.1723-74T>G ENSP00000426745.1:n.1723-74T>G
NM_000859.2:c.1723-74T>G NP_000850.1:n.1723-74T>G
NM_001130996.1:c.1564-74T>G NP_001124468.1:n.1564-74T>G
XM_011543357.1:c.1783-74T>G XP_011541659.1:n.1783-74T>G
XM_011543358.1:c.1723-74T>G XP_011541660.1:n.1723-74T>G
XM_011543359.1:c.1624-74T>G XP_011541661.1:n.1624-74T>G
NM_001364187.1:c.1723-74T>G NP_001351116.1:n.1723-74T>G
NM_000859.3:c.1723-74T>G MANE Select NP_000850.1:n.1723-74T>G
NM_001130996.2:c.1564-74T>G NP_001124468.1:n.1564-74T>G