Canonical Allele Identifier: CA2675943493
Gene: SLC26A2 HGNC NCBI

Linked Data

gnomAD v4: 5-149978400-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149978400C>A , CM000667.2:g.149978400C>A GRCh38
NC_000005.9:g.149357963C>A , CM000667.1:g.149357963C>A GRCh37
NC_000005.8:g.149338156C>A NCBI36
NG_007147.2:g.19518C>A , LRG_684:g.19518C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000690410.1:n.980C>A
ENST00000286298.5:c.699+49C>A MANE Select ENSP00000286298.4:n.699+49C>A
ENST00000286298.4:c.699+49C>A ENSP00000286298.4:n.699+49C>A
ENST00000503336.1:c.372+49C>A ENSP00000426053.1:n.372+49C>A
NM_000112.3:c.699+49C>A , LRG_684t1:c.699+49C>A NP_000103.2:n.699+49C>A
XM_017009191.2:c.699+49C>A XP_016864680.1:n.699+49C>A
NM_000112.4:c.699+49C>A MANE Select NP_000103.2:n.699+49C>A
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