Canonical Allele Identifier: CA151202237
Gene: SLC22A2 HGNC NCBI

Linked Data

dbSNP Id: rs150818356
gnomAD v2: 6-160670178-TAAGG-T
gnomAD v3: 6-160249146-TAAGG-T
gnomAD v4: 6-160249146-TAAGG-T
MyVariant Identifiers: chr6:g.160670179_160670182del (hg19) chr6:g.160249147_160249150del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160249151_160249154del , CM000668.2:g.160249151_160249154del GRCh38
NC_000006.11:g.160670183_160670186del , CM000668.1:g.160670183_160670186del GRCh37
NC_000006.10:g.160590173_160590176del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000366953.8:c.842+66_842+69del MANE Select ENSP00000355920.3:n.842+66_842+69del
ENST00000366952.1:c.779+66_779+69del ENSP00000355919.1:n.779+66_779+69del
ENST00000366953.7:c.842+66_842+69del ENSP00000355920.3:n.842+66_842+69del
ENST00000491092.1:n.739+66_739+69del
NM_003058.3:c.842+66_842+69del NP_003049.2:n.842+66_842+69del
NM_003058.4:c.842+66_842+69del MANE Select NP_003049.2:n.842+66_842+69del
Search 100 bp 5'
Search 100 bp 3'