Canonical Allele Identifier: CA1081635145

Gene: SLC22A5 MIR3936HG

Linked Data

• dbSNP Id: rs1751806332
• gnomAD v3: 5-132369772-T-C
• gnomAD v4: 5-132369772-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132369772T>C , CM000667.2:g.132369772T>C	GRCh38
NC_000005.9:g.131705464T>C , CM000667.1:g.131705464T>C	GRCh37
NC_000005.8:g.131733363T>C	NCBI36
NG_008982.1:g.5064T>C
NG_008982.2:g.5069T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000245407.8:c.-201T>C (SLC22A5) MANE Select	ENSP00000245407.3:n.-201T>C
ENST00000245407.7:c.-201T>C (SLC22A5)	ENSP00000245407.3:n.-201T>C
NM_001308122.1:c.-201T>C (SLC22A5)	NP_001295051.1:n.-201T>C
NM_003060.3:c.-201T>C (SLC22A5)	NP_003051.1:n.-201T>C
NR_110997.1:n.73+72A>G (MIR3936HG)
XR_427718.1:n.69T>C (SLC22A5)
XR_948290.1:n.69T>C (SLC22A5)
XR_948291.1:n.69T>C (SLC22A5)
XR_001742215.1:n.69T>C (SLC22A5)
XR_001742216.1:n.69T>C (SLC22A5)
XR_427718.2:n.69T>C (SLC22A5)
XR_948290.2:n.69T>C (SLC22A5)
XR_948291.2:n.69T>C (SLC22A5)
NM_003060.4:c.-201T>C (SLC22A5) MANE Select	NP_003051.1:n.-201T>C
NM_001308122.2:c.-201T>C (SLC22A5)	NP_001295051.1:n.-201T>C