Canonical Allele Identifier: CA1081635165

Gene: SLC22A5 MIR3936HG

Linked Data

• dbSNP Id: rs1751809074
• gnomAD v3: 5-132369814-C-G
• gnomAD v4: 5-132369814-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132369814C>G , CM000667.2:g.132369814C>G	GRCh38
NC_000005.9:g.131705506C>G , CM000667.1:g.131705506C>G	GRCh37
NC_000005.8:g.131733405C>G	NCBI36
NG_008982.1:g.5106C>G
NG_008982.2:g.5111C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245407.8:c.-159C>G (SLC22A5) MANE Select	ENSP00000245407.3:n.-159C>G
ENST00000245407.7:c.-159C>G (SLC22A5)	ENSP00000245407.3:n.-159C>G
NM_001308122.1:c.-159C>G (SLC22A5)	NP_001295051.1:n.-159C>G
NM_003060.3:c.-159C>G (SLC22A5)	NP_003051.1:n.-159C>G
NR_110997.1:n.73+30G>C (MIR3936HG)
XR_427718.1:n.111C>G (SLC22A5)
XR_948290.1:n.111C>G (SLC22A5)
XR_948291.1:n.111C>G (SLC22A5)
XR_001742215.1:n.111C>G (SLC22A5)
XR_001742216.1:n.111C>G (SLC22A5)
XR_427718.2:n.111C>G (SLC22A5)
XR_948290.2:n.111C>G (SLC22A5)
XR_948291.2:n.111C>G (SLC22A5)
NM_003060.4:c.-159C>G (SLC22A5) MANE Select	NP_003051.1:n.-159C>G
NM_001308122.2:c.-159C>G (SLC22A5)	NP_001295051.1:n.-159C>G