Canonical Allele Identifier: CA1590737310
Gene: SLC26A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149977843C= , CM000667.2:g.149977843C= GRCh38
NC_000005.9:g.149357406C= , CM000667.1:g.149357406C= GRCh37
NC_000005.8:g.149337599C= NCBI36
NG_007147.2:g.18961C= , LRG_684:g.18961C=

Transcript Alleles

HGVS Amino-acid change
ENST00000690410.1:n.423C=
ENST00000286298.5:c.191C= MANE Select ENSP00000286298.4:p.Thr64=
ENST00000286298.4:c.191C= ENSP00000286298.4:p.Thr64=
NM_000112.3:c.191C= , LRG_684t1:c.191C= NP_000103.2:p.Thr64=
XM_017009191.2:c.191C= XP_016864680.1:p.Thr64=
NM_000112.4:c.191C= MANE Select NP_000103.2:p.Thr64=