Canonical Allele Identifier: CA2255110715
Gene: SLC6A4 HGNC NCBI

Linked Data

dbSNP Id: rs1907219119

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30234771A>C , CM000679.2:g.30234771A>C GRCh38
NC_000017.10:g.28561789A>C , CM000679.1:g.28561789A>C GRCh37
NC_000017.9:g.25585915A>C NCBI36
NG_011747.2:g.6166T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000650711.1:c.-221+842T>G MANE Select ENSP00000498537.1:n.-221+842T>G
ENST00000261707.7:c.-221+842T>G ENSP00000261707.3:n.-221+842T>G
ENST00000394821.2:c.-221+842T>G ENSP00000378298.2:n.-221+842T>G
ENST00000401766.6:c.-124+842T>G ENSP00000385822.2:n.-124+842T>G
NM_001045.5:c.-221+842T>G NP_001036.1:n.-221+842T>G
NM_001045.6:c.-221+842T>G MANE Select NP_001036.1:n.-221+842T>G