Canonical Allele Identifier: CA2675943711
Gene: SLC26A2 HGNC NCBI

Linked Data

gnomAD v4: 5-149981910-A-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149981910A>T , CM000667.2:g.149981910A>T GRCh38
NC_000005.9:g.149361473A>T , CM000667.1:g.149361473A>T GRCh37
NC_000005.8:g.149341666A>T NCBI36
NG_007147.2:g.23028A>T , LRG_684:g.23028A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000286298.5:c.*97A>T MANE Select ENSP00000286298.4:n.*97A>T
ENST00000286298.4:c.*97A>T ENSP00000286298.4:n.*97A>T
ENST00000503336.1:c.372+3559A>T ENSP00000426053.1:n.372+3559A>T
NM_000112.3:c.*97A>T , LRG_684t1:c.*97A>T NP_000103.2:n.*97A>T
XM_017009191.2:c.*13-19A>T XP_016864680.1:n.*13-19A>T
NM_000112.4:c.*97A>T MANE Select NP_000103.2:n.*97A>T
Search 100 bp 5'
Search 100 bp 3'