Canonical Allele Identifier: CA1676974835
Gene: SLC22A2 HGNC NCBI

Linked Data

dbSNP Id: rs1783142464
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160249183_160249186del , CM000668.2:g.160249183_160249186del GRCh38
NC_000006.11:g.160670215_160670218del , CM000668.1:g.160670215_160670218del GRCh37
NC_000006.10:g.160590205_160590208del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000366953.8:c.842+32_842+35del MANE Select ENSP00000355920.3:n.842+32_842+35del
ENST00000366952.1:c.779+32_779+35del ENSP00000355919.1:n.779+32_779+35del
ENST00000366953.7:c.842+32_842+35del ENSP00000355920.3:n.842+32_842+35del
ENST00000491092.1:n.739+32_739+35del
NM_003058.3:c.842+32_842+35del NP_003049.2:n.842+32_842+35del
NM_003058.4:c.842+32_842+35del MANE Select NP_003049.2:n.842+32_842+35del
Search 100 bp 5'
Search 100 bp 3'