Canonical Allele Identifier: CA1082859065
Gene: SLC26A2 HGNC NCBI

Linked Data

dbSNP Id: rs1755116640
gnomAD v3: 5-149981994-A-G
gnomAD v4: 5-149981994-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149981994A>G , CM000667.2:g.149981994A>G GRCh38
NC_000005.9:g.149361557A>G , CM000667.1:g.149361557A>G GRCh37
NC_000005.8:g.149341750A>G NCBI36
NG_007147.2:g.23112A>G , LRG_684:g.23112A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000286298.5:c.*181A>G MANE Select ENSP00000286298.4:n.*181A>G
ENST00000286298.4:c.*181A>G ENSP00000286298.4:n.*181A>G
ENST00000503336.1:c.372+3643A>G ENSP00000426053.1:n.372+3643A>G
NM_000112.3:c.*181A>G , LRG_684t1:c.*181A>G NP_000103.2:n.*181A>G
XM_017009191.2:c.*78A>G XP_016864680.1:n.*78A>G
NM_000112.4:c.*181A>G MANE Select NP_000103.2:n.*181A>G
Search 100 bp 5'
Search 100 bp 3'