Canonical Allele Identifier: CA1590738975
Gene: SLC26A2 HGNC NCBI

Linked Data

dbSNP Id: rs1581232861
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149981850T>G , CM000667.2:g.149981850T>G GRCh38
NC_000005.9:g.149361413T>G , CM000667.1:g.149361413T>G GRCh37
NC_000005.8:g.149341606T>G NCBI36
NG_007147.2:g.22968T>G , LRG_684:g.22968T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000286298.5:c.*37T>G MANE Select ENSP00000286298.4:n.*37T>G
ENST00000286298.4:c.*37T>G ENSP00000286298.4:n.*37T>G
ENST00000503336.1:c.372+3499T>G ENSP00000426053.1:n.372+3499T>G
NM_000112.3:c.*37T>G , LRG_684t1:c.*37T>G NP_000103.2:n.*37T>G
XM_017009191.2:c.*12+25T>G XP_016864680.1:n.*12+25T>G
NM_000112.4:c.*37T>G MANE Select NP_000103.2:n.*37T>G
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