Canonical Allele Identifier: CA804782754
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs140094229
gnomAD v3: 5-1414398-TGG-T
gnomAD v4: 5-1414398-TGG-T
MyVariant Identifiers: chr5:g.1414514_1414515del (hg19) chr5:g.1414399_1414400del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1414404_1414405del , CM000667.2:g.1414404_1414405del GRCh38
NC_000005.9:g.1414519_1414520del , CM000667.1:g.1414519_1414520del GRCh37
NC_000005.8:g.1467519_1467520del NCBI36
NG_015885.1:g.36029_36030del

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1156+291_1156+292del MANE Select ENSP00000270349.9:n.1156+291_1156+292del
ENST00000270349.11:c.1156+291_1156+292del ENSP00000270349.9:n.1156+291_1156+292del
NM_001044.4:c.1156+291_1156+292del NP_001035.1:n.1156+291_1156+292del
NM_001044.5:c.1156+291_1156+292del MANE Select NP_001035.1:n.1156+291_1156+292del
Search 100 bp 5'
Search 100 bp 3'