Canonical Allele Identifier: CA447402020

Gene: SLC26A2

Linked Data

• MyVariant Identifiers: chr5:g.149357698T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149978135T>G , CM000667.2:g.149978135T>G	GRCh38
NC_000005.9:g.149357698T>G , CM000667.1:g.149357698T>G	GRCh37
NC_000005.8:g.149337891T>G	NCBI36
NG_007147.2:g.19253T>G , LRG_684:g.19253T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690410.1:n.715T>G
ENST00000286298.5:c.483T>G MANE Select	ENSP00000286298.4:p.Ser161=
ENST00000286298.4:c.483T>G	ENSP00000286298.4:p.Ser161=
ENST00000503336.1:c.156T>G	ENSP00000426053.1:p.Ser52=
NM_000112.3:c.483T>G , LRG_684t1:c.483T>G	NP_000103.2:p.Ser161=
XM_017009191.2:c.483T>G	XP_016864680.1:p.Ser161=
NM_000112.4:c.483T>G MANE Select	NP_000103.2:p.Ser161=