Canonical Allele Identifier: CA361705437
Gene: SLC26A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149978299G>A , CM000667.2:g.149978299G>A GRCh38
NC_000005.9:g.149357862G>A , CM000667.1:g.149357862G>A GRCh37
NC_000005.8:g.149338055G>A NCBI36
NG_007147.2:g.19417G>A , LRG_684:g.19417G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000690410.1:n.879G>A
ENST00000286298.5:c.647G>A MANE Select ENSP00000286298.4:p.Cys216Tyr
ENST00000286298.4:c.647G>A ENSP00000286298.4:p.Cys216Tyr
ENST00000503336.1:c.320G>A ENSP00000426053.1:p.Cys107Tyr
NM_000112.3:c.647G>A , LRG_684t1:c.647G>A NP_000103.2:p.Cys216Tyr
XM_017009191.2:c.647G>A XP_016864680.1:p.Cys216Tyr
NM_000112.4:c.647G>A MANE Select NP_000103.2:p.Cys216Tyr