Canonical Allele Identifier: CA1590738784
Gene: SLC26A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149981449G= , CM000667.2:g.149981449G= GRCh38
NC_000005.9:g.149361012G= , CM000667.1:g.149361012G= GRCh37
NC_000005.8:g.149341205G= NCBI36
NG_007147.2:g.22567G= , LRG_684:g.22567G=

Transcript Alleles

HGVS Amino-acid change
ENST00000286298.5:c.1856G= MANE Select ENSP00000286298.4:p.Arg619=
ENST00000286298.4:c.1856G= ENSP00000286298.4:p.Arg619=
ENST00000503336.1:c.372+3098G= ENSP00000426053.1:n.372+3098G=
NM_000112.3:c.1856G= , LRG_684t1:c.1856G= NP_000103.2:p.Arg619=
XM_017009191.2:c.1856G= XP_016864680.1:p.Arg619=
NM_000112.4:c.1856G= MANE Select NP_000103.2:p.Arg619=