Canonical Allele Identifier: CA499440101

Gene: SLC6A4

Linked Data

• MyVariant Identifiers: chr17:g.28548686C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30221668C>G , CM000679.2:g.30221668C>G	GRCh38
NC_000017.10:g.28548686C>G , CM000679.1:g.28548686C>G	GRCh37
NC_000017.9:g.25572812C>G	NCBI36
NG_011747.2:g.19269G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650711.1:c.291G>C MANE Select	ENSP00000498537.1:p.Val97=
ENST00000261707.7:c.291G>C	ENSP00000261707.3:p.Val97=
ENST00000394821.2:c.291G>C	ENSP00000378298.2:p.Val97=
ENST00000401766.6:c.291G>C	ENSP00000385822.2:p.Val97=
NM_001045.5:c.291G>C	NP_001036.1:p.Val97=
NM_001045.6:c.291G>C MANE Select	NP_001036.1:p.Val97=