Canonical Allele Identifier: CA359087139
Gene: SLC6A3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.1422016C>A (hg19) chr5:g.1421901C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1421901C>A , CM000667.2:g.1421901C>A GRCh38
NC_000005.9:g.1422016C>A , CM000667.1:g.1422016C>A GRCh37
NC_000005.8:g.1475016C>A NCBI36
NG_015885.1:g.28528G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000270349.12:c.767G>T MANE Select ENSP00000270349.9:p.Trp256Leu
ENST00000270349.11:c.767G>T ENSP00000270349.9:p.Trp256Leu
NM_001044.4:c.767G>T NP_001035.1:p.Trp256Leu
NM_001044.5:c.767G>T MANE Select NP_001035.1:p.Trp256Leu
Search 100 bp 5'
Search 100 bp 3'