Canonical Allele Identifier: CA2681069966
Gene: SLC22A2 HGNC NCBI

Linked Data

gnomAD v4: 6-160249199-A-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160249199A>T , CM000668.2:g.160249199A>T GRCh38
NC_000006.11:g.160670231A>T , CM000668.1:g.160670231A>T GRCh37
NC_000006.10:g.160590221A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000366953.8:c.842+17T>A MANE Select ENSP00000355920.3:n.842+17T>A
ENST00000366952.1:c.779+17T>A ENSP00000355919.1:n.779+17T>A
ENST00000366953.7:c.842+17T>A ENSP00000355920.3:n.842+17T>A
ENST00000491092.1:n.739+17T>A
NM_003058.3:c.842+17T>A NP_003049.2:n.842+17T>A
NM_003058.4:c.842+17T>A MANE Select NP_003049.2:n.842+17T>A
Search 100 bp 5'
Search 100 bp 3'