Canonical Allele Identifier: CA4084527
Gene: SLC22A2 HGNC NCBI

Linked Data

dbSNP Id: rs759402281
ExAC: 6:160670203 A / T
gnomAD v2: 6-160670203-A-T
gnomAD v4: 6-160249171-A-T
MyVariant Identifiers: chr6:g.160670203A>T (hg19) chr6:g.160249171A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160249171A>T , CM000668.2:g.160249171A>T GRCh38
NC_000006.11:g.160670203A>T , CM000668.1:g.160670203A>T GRCh37
NC_000006.10:g.160590193A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000366953.8:c.842+45T>A MANE Select ENSP00000355920.3:n.842+45T>A
ENST00000366952.1:c.779+45T>A ENSP00000355919.1:n.779+45T>A
ENST00000366953.7:c.842+45T>A ENSP00000355920.3:n.842+45T>A
ENST00000491092.1:n.739+45T>A
NM_003058.3:c.842+45T>A NP_003049.2:n.842+45T>A
NM_003058.4:c.842+45T>A MANE Select NP_003049.2:n.842+45T>A
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