Canonical Allele Identifier: CA1590737579
Gene: SLC26A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149978529G= , CM000667.2:g.149978529G= GRCh38
NC_000005.9:g.149358092G= , CM000667.1:g.149358092G= GRCh37
NC_000005.8:g.149338285G= NCBI36
NG_007147.2:g.19647G= , LRG_684:g.19647G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000690410.1:n.1109G=
ENST00000286298.5:c.699+178G= MANE Select ENSP00000286298.4:n.699+178G=
ENST00000286298.4:c.699+178G= ENSP00000286298.4:n.699+178G=
ENST00000503336.1:c.372+178G= ENSP00000426053.1:n.372+178G=
NM_000112.3:c.699+178G= , LRG_684t1:c.699+178G= NP_000103.2:n.699+178G=
XM_017009191.2:c.699+178G= XP_016864680.1:n.699+178G=
NM_000112.4:c.699+178G= MANE Select NP_000103.2:n.699+178G=
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