Canonical Allele Identifier: CA361705019
Gene: SLC26A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149978102T>G , CM000667.2:g.149978102T>G GRCh38
NC_000005.9:g.149357665T>G , CM000667.1:g.149357665T>G GRCh37
NC_000005.8:g.149337858T>G NCBI36
NG_007147.2:g.19220T>G , LRG_684:g.19220T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000690410.1:n.682T>G
ENST00000286298.5:c.450T>G MANE Select ENSP00000286298.4:p.Ile150Met
ENST00000286298.4:c.450T>G ENSP00000286298.4:p.Ile150Met
ENST00000503336.1:c.123T>G ENSP00000426053.1:p.Ile41Met
NM_000112.3:c.450T>G , LRG_684t1:c.450T>G NP_000103.2:p.Ile150Met
XM_017009191.2:c.450T>G XP_016864680.1:p.Ile150Met
NM_000112.4:c.450T>G MANE Select NP_000103.2:p.Ile150Met