Canonical Allele Identifier: CA361704773
Gene: SLC26A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149977985T>G , CM000667.2:g.149977985T>G GRCh38
NC_000005.9:g.149357548T>G , CM000667.1:g.149357548T>G GRCh37
NC_000005.8:g.149337741T>G NCBI36
NG_007147.2:g.19103T>G , LRG_684:g.19103T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000690410.1:n.565T>G
ENST00000286298.5:c.333T>G MANE Select ENSP00000286298.4:p.Asp111Glu
ENST00000286298.4:c.333T>G ENSP00000286298.4:p.Asp111Glu
ENST00000503336.1:c.6T>G ENSP00000426053.1:p.Asp2Glu
NM_000112.3:c.333T>G , LRG_684t1:c.333T>G NP_000103.2:p.Asp111Glu
XM_017009191.2:c.333T>G XP_016864680.1:p.Asp111Glu
NM_000112.4:c.333T>G MANE Select NP_000103.2:p.Asp111Glu