Canonical Allele Identifier: CA361707536
Gene: SLC26A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.149360433T>G (hg19) chr5:g.149980870T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149980870T>G , CM000667.2:g.149980870T>G GRCh38
NC_000005.9:g.149360433T>G , CM000667.1:g.149360433T>G GRCh37
NC_000005.8:g.149340626T>G NCBI36
NG_007147.2:g.21988T>G , LRG_684:g.21988T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000286298.5:c.1277T>G MANE Select ENSP00000286298.4:p.Ile426Ser
ENST00000286298.4:c.1277T>G ENSP00000286298.4:p.Ile426Ser
ENST00000503336.1:c.372+2519T>G ENSP00000426053.1:n.372+2519T>G
NM_000112.3:c.1277T>G , LRG_684t1:c.1277T>G NP_000103.2:p.Ile426Ser
XM_017009191.2:c.1277T>G XP_016864680.1:p.Ile426Ser
NM_000112.4:c.1277T>G MANE Select NP_000103.2:p.Ile426Ser
Search 100 bp 5'
Search 100 bp 3'