Canonical Allele Identifier: CA1522626449
Gene: SLC6A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1414289G= , CM000667.2:g.1414289G= GRCh38
NC_000005.9:g.1414404G= , CM000667.1:g.1414404G= GRCh37
NC_000005.8:g.1467404G= NCBI36
NG_015885.1:g.36140C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1156+402C= MANE Select ENSP00000270349.9:n.1156+402C=
ENST00000270349.11:c.1156+402C= ENSP00000270349.9:n.1156+402C=
NM_001044.4:c.1156+402C= NP_001035.1:n.1156+402C=
NM_001044.5:c.1156+402C= MANE Select NP_001035.1:n.1156+402C=