Canonical Allele Identifier: CA1590738829
Gene: SLC26A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149981559A= , CM000667.2:g.149981559A= GRCh38
NC_000005.9:g.149361122A= , CM000667.1:g.149361122A= GRCh37
NC_000005.8:g.149341315A= NCBI36
NG_007147.2:g.22677A= , LRG_684:g.22677A=

Transcript Alleles

HGVS Amino-acid change
ENST00000286298.5:c.1966A= MANE Select ENSP00000286298.4:p.Ile656=
ENST00000286298.4:c.1966A= ENSP00000286298.4:p.Ile656=
ENST00000503336.1:c.372+3208A= ENSP00000426053.1:n.372+3208A=
NM_000112.3:c.1966A= , LRG_684t1:c.1966A= NP_000103.2:p.Ile656=
XM_017009191.2:c.1966A= XP_016864680.1:p.Ile656=
NM_000112.4:c.1966A= MANE Select NP_000103.2:p.Ile656=