Canonical Allele Identifier: CA359083761
Gene: SLC6A3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.1416212C>G (hg19) chr5:g.1416097C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1416097C>G , CM000667.2:g.1416097C>G GRCh38
NC_000005.9:g.1416212C>G , CM000667.1:g.1416212C>G GRCh37
NC_000005.8:g.1469212C>G NCBI36
NG_015885.1:g.34332G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000270349.12:c.1031+1G>C MANE Select ENSP00000270349.9:n.1031+1G>C
ENST00000270349.11:c.1031+1G>C ENSP00000270349.9:n.1031+1G>C
ENST00000511750.1:n.481+1G>C
NM_001044.4:c.1031+1G>C NP_001035.1:n.1031+1G>C
NM_001044.5:c.1031+1G>C MANE Select NP_001035.1:n.1031+1G>C
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