Canonical Allele Identifier: CA1590737416
Gene: SLC26A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149978124C= , CM000667.2:g.149978124C= GRCh38
NC_000005.9:g.149357687C= , CM000667.1:g.149357687C= GRCh37
NC_000005.8:g.149337880C= NCBI36
NG_007147.2:g.19242C= , LRG_684:g.19242C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000690410.1:n.704C=
ENST00000286298.5:c.472C= MANE Select ENSP00000286298.4:p.Arg158=
ENST00000286298.4:c.472C= ENSP00000286298.4:p.Arg158=
ENST00000503336.1:c.145C= ENSP00000426053.1:p.Arg49=
NM_000112.3:c.472C= , LRG_684t1:c.472C= NP_000103.2:p.Arg158=
XM_017009191.2:c.472C= XP_016864680.1:p.Arg158=
NM_000112.4:c.472C= MANE Select NP_000103.2:p.Arg158=