Canonical Allele Identifier: CA2255110677
Gene: SLC6A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30234674A= , CM000679.2:g.30234674A= GRCh38
NC_000017.10:g.28561692A= , CM000679.1:g.28561692A= GRCh37
NC_000017.9:g.25585818A= NCBI36
NG_011747.2:g.6263T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650711.1:c.-221+939T= MANE Select ENSP00000498537.1:n.-221+939T=
ENST00000261707.7:c.-221+939T= ENSP00000261707.3:n.-221+939T=
ENST00000394821.2:c.-221+939T= ENSP00000378298.2:n.-221+939T=
ENST00000401766.6:c.-124+939T= ENSP00000385822.2:n.-124+939T=
NM_001045.5:c.-221+939T= NP_001036.1:n.-221+939T=
NM_001045.6:c.-221+939T= MANE Select NP_001036.1:n.-221+939T=