Canonical Allele Identifier: CA218757897
Gene: SLC17A6 HGNC NCBI

Linked Data

dbSNP Id: rs1900586
gnomAD v2: 11-22387440-T-C
gnomAD v3: 11-22365894-T-C
gnomAD v4: 11-22365894-T-C
MyVariant Identifiers: chr11:g.22387440T>C (hg19) chr11:g.22365894T>C (hg38)
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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
Search 100 bp 5'
Search 100 bp 3'