Canonical Allele Identifier: CA2675943478
Gene: SLC26A2 HGNC NCBI

Linked Data

gnomAD v4: 5-149978364-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149978364G>A , CM000667.2:g.149978364G>A GRCh38
NC_000005.9:g.149357927G>A , CM000667.1:g.149357927G>A GRCh37
NC_000005.8:g.149338120G>A NCBI36
NG_007147.2:g.19482G>A , LRG_684:g.19482G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000690410.1:n.944G>A
ENST00000286298.5:c.699+13G>A MANE Select ENSP00000286298.4:n.699+13G>A
ENST00000286298.4:c.699+13G>A ENSP00000286298.4:n.699+13G>A
ENST00000503336.1:c.372+13G>A ENSP00000426053.1:n.372+13G>A
NM_000112.3:c.699+13G>A , LRG_684t1:c.699+13G>A NP_000103.2:n.699+13G>A
XM_017009191.2:c.699+13G>A XP_016864680.1:n.699+13G>A
NM_000112.4:c.699+13G>A MANE Select NP_000103.2:n.699+13G>A
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