Canonical Allele Identifier: CA804997488
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1342241125
MyVariant Identifiers: chr5:g.1443745G>C (hg19) chr5:g.1443630G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1443630G>C , CM000667.2:g.1443630G>C GRCh38
NC_000005.9:g.1443745G>C , CM000667.1:g.1443745G>C GRCh37
NC_000005.8:g.1496745G>C NCBI36
NG_015885.1:g.6799C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.-45-388C>G MANE Select ENSP00000270349.9:n.-45-388C>G
ENST00000270349.11:c.-45-388C>G ENSP00000270349.9:n.-45-388C>G
NM_001044.4:c.-45-388C>G NP_001035.1:n.-45-388C>G
NM_001044.5:c.-45-388C>G MANE Select NP_001035.1:n.-45-388C>G
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