Canonical Allele Identifier: CA1522626453
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1756200750
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1414292G>C , CM000667.2:g.1414292G>C GRCh38
NC_000005.9:g.1414407G>C , CM000667.1:g.1414407G>C GRCh37
NC_000005.8:g.1467407G>C NCBI36
NG_015885.1:g.36137C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1156+399C>G MANE Select ENSP00000270349.9:n.1156+399C>G
ENST00000270349.11:c.1156+399C>G ENSP00000270349.9:n.1156+399C>G
NM_001044.4:c.1156+399C>G NP_001035.1:n.1156+399C>G
NM_001044.5:c.1156+399C>G MANE Select NP_001035.1:n.1156+399C>G
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