Canonical Allele Identifier: CA2675943685
Gene: SLC26A2 HGNC NCBI

Linked Data

gnomAD v4: 5-149981860-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149981860A>G , CM000667.2:g.149981860A>G GRCh38
NC_000005.9:g.149361423A>G , CM000667.1:g.149361423A>G GRCh37
NC_000005.8:g.149341616A>G NCBI36
NG_007147.2:g.22978A>G , LRG_684:g.22978A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000286298.5:c.*47A>G MANE Select ENSP00000286298.4:n.*47A>G
ENST00000286298.4:c.*47A>G ENSP00000286298.4:n.*47A>G
ENST00000503336.1:c.372+3509A>G ENSP00000426053.1:n.372+3509A>G
NM_000112.3:c.*47A>G , LRG_684t1:c.*47A>G NP_000103.2:n.*47A>G
XM_017009191.2:c.*12+35A>G XP_016864680.1:n.*12+35A>G
NM_000112.4:c.*47A>G MANE Select NP_000103.2:n.*47A>G
Search 100 bp 5'
Search 100 bp 3'