Canonical Allele Identifier: CA361704390

Gene: SLC26A2

Linked Data

• MyVariant Identifiers: chr5:g.149357427T>G (hg19) ; chr5:g.149977864T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149977864T>G , CM000667.2:g.149977864T>G	GRCh38
NC_000005.9:g.149357427T>G , CM000667.1:g.149357427T>G	GRCh37
NC_000005.8:g.149337620T>G	NCBI36
NG_007147.2:g.18982T>G , LRG_684:g.18982T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000690410.1:n.444T>G
ENST00000286298.5:c.212T>G MANE Select	ENSP00000286298.4:p.Ile71Ser
ENST00000286298.4:c.212T>G	ENSP00000286298.4:p.Ile71Ser
NM_000112.3:c.212T>G , LRG_684t1:c.212T>G	NP_000103.2:p.Ile71Ser
XM_017009191.2:c.212T>G	XP_016864680.1:p.Ile71Ser
NM_000112.4:c.212T>G MANE Select	NP_000103.2:p.Ile71Ser