Canonical Allele Identifier: CA447402924
Gene: SLC26A2 HGNC NCBI

Linked Data

dbSNP Id: rs1755100727
MyVariant Identifiers: chr5:g.149361058A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149981495A>G , CM000667.2:g.149981495A>G GRCh38
NC_000005.9:g.149361058A>G , CM000667.1:g.149361058A>G GRCh37
NC_000005.8:g.149341251A>G NCBI36
NG_007147.2:g.22613A>G , LRG_684:g.22613A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000286298.5:c.1902A>G MANE Select ENSP00000286298.4:p.Glu634=
ENST00000286298.4:c.1902A>G ENSP00000286298.4:p.Glu634=
ENST00000503336.1:c.372+3144A>G ENSP00000426053.1:n.372+3144A>G
NM_000112.3:c.1902A>G , LRG_684t1:c.1902A>G NP_000103.2:p.Glu634=
XM_017009191.2:c.1902A>G XP_016864680.1:p.Glu634=
NM_000112.4:c.1902A>G MANE Select NP_000103.2:p.Glu634=
Search 100 bp 5'
Search 100 bp 3'