Canonical Allele Identifier: CA1590737278
Gene: SLC26A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149977767T= , CM000667.2:g.149977767T= GRCh38
NC_000005.9:g.149357330T= , CM000667.1:g.149357330T= GRCh37
NC_000005.8:g.149337523T= NCBI36
NG_007147.2:g.18885T= , LRG_684:g.18885T=

Transcript Alleles

HGVS Amino-acid change
ENST00000690410.1:n.347T=
ENST00000286298.5:c.115T= MANE Select ENSP00000286298.4:p.Phe39=
ENST00000286298.4:c.115T= ENSP00000286298.4:p.Phe39=
NM_000112.3:c.115T= , LRG_684t1:c.115T= NP_000103.2:p.Phe39=
XM_017009191.2:c.115T= XP_016864680.1:p.Phe39=
NM_000112.4:c.115T= MANE Select NP_000103.2:p.Phe39=