Canonical Allele Identifier: CA1522626601
Gene: SLC6A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1414392A= , CM000667.2:g.1414392A= GRCh38
NC_000005.9:g.1414507A= , CM000667.1:g.1414507A= GRCh37
NC_000005.8:g.1467507A= NCBI36
NG_015885.1:g.36037T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1156+299T= MANE Select ENSP00000270349.9:n.1156+299T=
ENST00000270349.11:c.1156+299T= ENSP00000270349.9:n.1156+299T=
NM_001044.4:c.1156+299T= NP_001035.1:n.1156+299T=
NM_001044.5:c.1156+299T= MANE Select NP_001035.1:n.1156+299T=