Canonical Allele Identifier: CA447401807
Gene: SLC26A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.149357407A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149977844A>T , CM000667.2:g.149977844A>T GRCh38
NC_000005.9:g.149357407A>T , CM000667.1:g.149357407A>T GRCh37
NC_000005.8:g.149337600A>T NCBI36
NG_007147.2:g.18962A>T , LRG_684:g.18962A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000690410.1:n.424A>T
ENST00000286298.5:c.192A>T MANE Select ENSP00000286298.4:p.Thr64=
ENST00000286298.4:c.192A>T ENSP00000286298.4:p.Thr64=
NM_000112.3:c.192A>T , LRG_684t1:c.192A>T NP_000103.2:p.Thr64=
XM_017009191.2:c.192A>T XP_016864680.1:p.Thr64=
NM_000112.4:c.192A>T MANE Select NP_000103.2:p.Thr64=
Search 100 bp 5'
Search 100 bp 3'