Canonical Allele Identifier: CA805532951
Gene: SLC26A2 HGNC NCBI

Linked Data

dbSNP Id: rs1422096637
gnomAD v4: 5-149981963-A-G
MyVariant Identifiers: chr5:g.149361526A>G (hg19) chr5:g.149981963A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149981963A>G , CM000667.2:g.149981963A>G GRCh38
NC_000005.9:g.149361526A>G , CM000667.1:g.149361526A>G GRCh37
NC_000005.8:g.149341719A>G NCBI36
NG_007147.2:g.23081A>G , LRG_684:g.23081A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000286298.5:c.*150A>G MANE Select ENSP00000286298.4:n.*150A>G
ENST00000286298.4:c.*150A>G ENSP00000286298.4:n.*150A>G
ENST00000503336.1:c.372+3612A>G ENSP00000426053.1:n.372+3612A>G
NM_000112.3:c.*150A>G , LRG_684t1:c.*150A>G NP_000103.2:n.*150A>G
XM_017009191.2:c.*47A>G XP_016864680.1:n.*47A>G
NM_000112.4:c.*150A>G MANE Select NP_000103.2:n.*150A>G
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