Canonical Allele Identifier: CA361706697
Gene: SLC26A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149980572T>A , CM000667.2:g.149980572T>A GRCh38
NC_000005.9:g.149360135T>A , CM000667.1:g.149360135T>A GRCh37
NC_000005.8:g.149340328T>A NCBI36
NG_007147.2:g.21690T>A , LRG_684:g.21690T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000286298.5:c.979T>A MANE Select ENSP00000286298.4:p.Ser327Thr
ENST00000286298.4:c.979T>A ENSP00000286298.4:p.Ser327Thr
ENST00000503336.1:c.372+2221T>A ENSP00000426053.1:n.372+2221T>A
NM_000112.3:c.979T>A , LRG_684t1:c.979T>A NP_000103.2:p.Ser327Thr
XM_017009191.2:c.979T>A XP_016864680.1:p.Ser327Thr
NM_000112.4:c.979T>A MANE Select NP_000103.2:p.Ser327Thr