Canonical Allele Identifier: CA1590737419
Gene: SLC26A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149978129C= , CM000667.2:g.149978129C= GRCh38
NC_000005.9:g.149357692C= , CM000667.1:g.149357692C= GRCh37
NC_000005.8:g.149337885C= NCBI36
NG_007147.2:g.19247C= , LRG_684:g.19247C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000690410.1:n.709C=
ENST00000286298.5:c.477C= MANE Select ENSP00000286298.4:p.His159=
ENST00000286298.4:c.477C= ENSP00000286298.4:p.His159=
ENST00000503336.1:c.150C= ENSP00000426053.1:p.His50=
NM_000112.3:c.477C= , LRG_684t1:c.477C= NP_000103.2:p.His159=
XM_017009191.2:c.477C= XP_016864680.1:p.His159=
NM_000112.4:c.477C= MANE Select NP_000103.2:p.His159=