Canonical Allele Identifier: CA447149109
Gene: SLC26A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.149361199T>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149981636T>G , CM000667.2:g.149981636T>G GRCh38
NC_000005.9:g.149361199T>G , CM000667.1:g.149361199T>G GRCh37
NC_000005.8:g.149341392T>G NCBI36
NG_007147.2:g.22754T>G , LRG_684:g.22754T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000286298.5:c.2043T>G MANE Select ENSP00000286298.4:p.Val681=
ENST00000286298.4:c.2043T>G ENSP00000286298.4:p.Val681=
ENST00000503336.1:c.372+3285T>G ENSP00000426053.1:n.372+3285T>G
NM_000112.3:c.2043T>G , LRG_684t1:c.2043T>G NP_000103.2:p.Val681=
XM_017009191.2:c.2043T>G XP_016864680.1:p.Val681=
NM_000112.4:c.2043T>G MANE Select NP_000103.2:p.Val681=
Search 100 bp 5'
Search 100 bp 3'