Canonical Allele Identifier: CA3505222
Gene: SLC26A2 HGNC NCBI

Linked Data

dbSNP Id: rs377685351

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149977874G>A , CM000667.2:g.149977874G>A GRCh38
NC_000005.9:g.149357437G>A , CM000667.1:g.149357437G>A GRCh37
NC_000005.8:g.149337630G>A NCBI36
NG_007147.2:g.18992G>A , LRG_684:g.18992G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000690410.1:n.454G>A
ENST00000286298.5:c.222G>A MANE Select ENSP00000286298.4:p.Leu74=
ENST00000286298.4:c.222G>A ENSP00000286298.4:p.Leu74=
NM_000112.3:c.222G>A , LRG_684t1:c.222G>A NP_000103.2:p.Leu74=
XM_017009191.2:c.222G>A XP_016864680.1:p.Leu74=
NM_000112.4:c.222G>A MANE Select NP_000103.2:p.Leu74=