Canonical Allele Identifier: CA2673093872
Gene: SLC6A3 HGNC NCBI

Linked Data

gnomAD v4: 5-1394895-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1394895G>T , CM000667.2:g.1394895G>T GRCh38
NC_000005.9:g.1395010G>T , CM000667.1:g.1395010G>T GRCh37
NC_000005.8:g.1448010G>T NCBI36
NG_015885.1:g.55534C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1840-137C>A MANE Select ENSP00000270349.9:n.1840-137C>A
ENST00000270349.11:c.1840-137C>A ENSP00000270349.9:n.1840-137C>A
ENST00000512002.2:n.221-137C>A
NM_001044.4:c.1840-137C>A NP_001035.1:n.1840-137C>A
NM_001044.5:c.1840-137C>A MANE Select NP_001035.1:n.1840-137C>A