Canonical Allele Identifier: CA562767610

Gene: SLC22A5 MIR3936HG

Linked Data

• dbSNP Id: rs1259331982
• gnomAD v2: 5-131705428-C-G
• gnomAD v3: 5-132369736-C-G
• gnomAD v4: 5-132369736-C-G
• MyVariant Identifiers: chr5:g.131705428C>G (hg19) ; chr5:g.132369736C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132369736C>G , CM000667.2:g.132369736C>G	GRCh38
NC_000005.9:g.131705428C>G , CM000667.1:g.131705428C>G	GRCh37
NC_000005.8:g.131733327C>G	NCBI36
NG_008982.1:g.5028C>G
NG_008982.2:g.5033C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245407.8:c.-237C>G (SLC22A5) MANE Select	ENSP00000245407.3:n.-237C>G
NM_001308122.1:c.-237C>G (SLC22A5)	NP_001295051.1:n.-237C>G
NM_003060.3:c.-237C>G (SLC22A5)	NP_003051.1:n.-237C>G
NR_110997.1:n.73+108G>C (MIR3936HG)
XR_427718.1:n.33C>G (SLC22A5)
XR_948290.1:n.33C>G (SLC22A5)
XR_948291.1:n.33C>G (SLC22A5)
XR_001742215.1:n.33C>G (SLC22A5)
XR_001742216.1:n.33C>G (SLC22A5)
XR_427718.2:n.33C>G (SLC22A5)
XR_948290.2:n.33C>G (SLC22A5)
XR_948291.2:n.33C>G (SLC22A5)
NM_003060.4:c.-237C>G (SLC22A5) MANE Select	NP_003051.1:n.-237C>G
NM_001308122.2:c.-237C>G (SLC22A5)	NP_001295051.1:n.-237C>G