Canonical Allele Identifier: CA112968503
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1025227989
gnomAD v2: 5-1423774-C-G
gnomAD v3: 5-1423659-C-G
gnomAD v4: 5-1423659-C-G
MyVariant Identifiers: chr5:g.1423774C>G (hg19) chr5:g.1423659C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1423659C>G , CM000667.2:g.1423659C>G GRCh38
NC_000005.9:g.1423774C>G , CM000667.1:g.1423774C>G GRCh37
NC_000005.8:g.1476774C>G NCBI36
NG_015885.1:g.26770G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000270349.12:c.654-1645G>C MANE Select ENSP00000270349.9:n.654-1645G>C
ENST00000270349.11:c.654-1645G>C ENSP00000270349.9:n.654-1645G>C
NM_001044.4:c.654-1645G>C NP_001035.1:n.654-1645G>C
NM_001044.5:c.654-1645G>C MANE Select NP_001035.1:n.654-1645G>C
Search 100 bp 5'
Search 100 bp 3'