Canonical Allele Identifier: CA361704914
Gene: SLC26A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149978053G>T , CM000667.2:g.149978053G>T GRCh38
NC_000005.9:g.149357616G>T , CM000667.1:g.149357616G>T GRCh37
NC_000005.8:g.149337809G>T NCBI36
NG_007147.2:g.19171G>T , LRG_684:g.19171G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000690410.1:n.633G>T
ENST00000286298.5:c.401G>T MANE Select ENSP00000286298.4:p.Gly134Val
ENST00000286298.4:c.401G>T ENSP00000286298.4:p.Gly134Val
ENST00000503336.1:c.74G>T ENSP00000426053.1:p.Gly25Val
NM_000112.3:c.401G>T , LRG_684t1:c.401G>T NP_000103.2:p.Gly134Val
XM_017009191.2:c.401G>T XP_016864680.1:p.Gly134Val
NM_000112.4:c.401G>T MANE Select NP_000103.2:p.Gly134Val