Canonical Allele Identifier: CA1590737558
Gene: SLC26A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149978473T= , CM000667.2:g.149978473T= GRCh38
NC_000005.9:g.149358036T= , CM000667.1:g.149358036T= GRCh37
NC_000005.8:g.149338229T= NCBI36
NG_007147.2:g.19591T= , LRG_684:g.19591T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000690410.1:n.1053T=
ENST00000286298.5:c.699+122T= MANE Select ENSP00000286298.4:n.699+122T=
ENST00000286298.4:c.699+122T= ENSP00000286298.4:n.699+122T=
ENST00000503336.1:c.372+122T= ENSP00000426053.1:n.372+122T=
NM_000112.3:c.699+122T= , LRG_684t1:c.699+122T= NP_000103.2:n.699+122T=
XM_017009191.2:c.699+122T= XP_016864680.1:n.699+122T=
NM_000112.4:c.699+122T= MANE Select NP_000103.2:n.699+122T=
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