Canonical Allele Identifier: CA361708902
Gene: SLC26A2 HGNC NCBI

Linked Data

dbSNP Id: rs1330735657

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149981407A>G , CM000667.2:g.149981407A>G GRCh38
NC_000005.9:g.149360970A>G , CM000667.1:g.149360970A>G GRCh37
NC_000005.8:g.149341163A>G NCBI36
NG_007147.2:g.22525A>G , LRG_684:g.22525A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000286298.5:c.1814A>G MANE Select ENSP00000286298.4:p.Asn605Ser
ENST00000286298.4:c.1814A>G ENSP00000286298.4:p.Asn605Ser
ENST00000503336.1:c.372+3056A>G ENSP00000426053.1:n.372+3056A>G
NM_000112.3:c.1814A>G , LRG_684t1:c.1814A>G NP_000103.2:p.Asn605Ser
XM_017009191.2:c.1814A>G XP_016864680.1:p.Asn605Ser
NM_000112.4:c.1814A>G MANE Select NP_000103.2:p.Asn605Ser