Canonical Allele Identifier: CA218757897

Gene: SLC17A6

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22365894T>C , CM000673.2:g.22365894T>C	GRCh38
NC_000011.9:g.22387440T>C , CM000673.1:g.22387440T>C	GRCh37
NC_000011.8:g.22344016T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263160.4:c.891+205T>C MANE Select	ENSP00000263160.3:n.891+205T>C
ENST00000648880.1:n.574T>C
ENST00000263160.3:c.891+205T>C	ENSP00000263160.3:n.891+205T>C
NM_020346.2:c.891+205T>C	NP_065079.1:n.891+205T>C
NM_020346.3:c.891+205T>C MANE Select	NP_065079.1:n.891+205T>C