Canonical Allele Identifier: CA1590737607
Gene: SLC26A2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149978590T= , CM000667.2:g.149978590T= GRCh38
NC_000005.9:g.149358153T= , CM000667.1:g.149358153T= GRCh37
NC_000005.8:g.149338346T= NCBI36
NG_007147.2:g.19708T= , LRG_684:g.19708T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000690410.1:n.1170T=
ENST00000286298.5:c.699+239T= MANE Select ENSP00000286298.4:n.699+239T=
ENST00000286298.4:c.699+239T= ENSP00000286298.4:n.699+239T=
ENST00000503336.1:c.372+239T= ENSP00000426053.1:n.372+239T=
NM_000112.3:c.699+239T= , LRG_684t1:c.699+239T= NP_000103.2:n.699+239T=
XM_017009191.2:c.699+239T= XP_016864680.1:n.699+239T=
NM_000112.4:c.699+239T= MANE Select NP_000103.2:n.699+239T=
Search 100 bp 5'
Search 100 bp 3'