Canonical Allele Identifier: CA803980080
Gene: SLC22A5 HGNC NCBI
MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs1338260764

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369827T>C , CM000667.2:g.132369827T>C GRCh38
NC_000005.9:g.131705519T>C , CM000667.1:g.131705519T>C GRCh37
NC_000005.8:g.131733418T>C NCBI36
NG_008982.1:g.5119T>C
NG_008982.2:g.5124T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000435065.7:c.-146T>C (SLC22A5) ENSP00000402760.2:n.-146T>C
ENST00000245407.8:c.-146T>C (SLC22A5) MANE Select ENSP00000245407.3:n.-146T>C
ENST00000245407.7:c.-146T>C (SLC22A5) ENSP00000245407.3:n.-146T>C
NM_001308122.1:c.-146T>C (SLC22A5) NP_001295051.1:n.-146T>C
NM_003060.3:c.-146T>C (SLC22A5) NP_003051.1:n.-146T>C
NR_110997.1:n.73+17A>G (MIR3936HG)
XR_427718.1:n.124T>C (SLC22A5)
XR_948290.1:n.124T>C (SLC22A5)
XR_948291.1:n.124T>C (SLC22A5)
XR_001742215.1:n.124T>C (SLC22A5)
XR_001742216.1:n.124T>C (SLC22A5)
XR_427718.2:n.124T>C (SLC22A5)
XR_948290.2:n.124T>C (SLC22A5)
XR_948291.2:n.124T>C (SLC22A5)
NM_003060.4:c.-146T>C (SLC22A5) MANE Select NP_003051.1:n.-146T>C
NM_001308122.2:c.-146T>C (SLC22A5) NP_001295051.1:n.-146T>C