Canonical Allele Identifier: CA2675943745
Gene: SLC26A2 HGNC NCBI

Linked Data

gnomAD v4: 5-149981971-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149981971A>G , CM000667.2:g.149981971A>G GRCh38
NC_000005.9:g.149361534A>G , CM000667.1:g.149361534A>G GRCh37
NC_000005.8:g.149341727A>G NCBI36
NG_007147.2:g.23089A>G , LRG_684:g.23089A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000286298.5:c.*158A>G MANE Select ENSP00000286298.4:n.*158A>G
ENST00000286298.4:c.*158A>G ENSP00000286298.4:n.*158A>G
ENST00000503336.1:c.372+3620A>G ENSP00000426053.1:n.372+3620A>G
NM_000112.3:c.*158A>G , LRG_684t1:c.*158A>G NP_000103.2:n.*158A>G
XM_017009191.2:c.*55A>G XP_016864680.1:n.*55A>G
NM_000112.4:c.*158A>G MANE Select NP_000103.2:n.*158A>G
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