Canonical Allele Identifier: CA129082882
Gene: SLC26A2 HGNC NCBI

Linked Data

dbSNP Id: rs916481680
gnomAD v3: 5-149978527-A-G
gnomAD v4: 5-149978527-A-G
MyVariant Identifiers: chr5:g.149358090A>G (hg19) chr5:g.149978527A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149978527A>G , CM000667.2:g.149978527A>G GRCh38
NC_000005.9:g.149358090A>G , CM000667.1:g.149358090A>G GRCh37
NC_000005.8:g.149338283A>G NCBI36
NG_007147.2:g.19645A>G , LRG_684:g.19645A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000690410.1:n.1107A>G
ENST00000286298.5:c.699+176A>G MANE Select ENSP00000286298.4:n.699+176A>G
ENST00000286298.4:c.699+176A>G ENSP00000286298.4:n.699+176A>G
ENST00000503336.1:c.372+176A>G ENSP00000426053.1:n.372+176A>G
NM_000112.3:c.699+176A>G , LRG_684t1:c.699+176A>G NP_000103.2:n.699+176A>G
XM_017009191.2:c.699+176A>G XP_016864680.1:n.699+176A>G
NM_000112.4:c.699+176A>G MANE Select NP_000103.2:n.699+176A>G
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