Canonical Allele Identifier: CA361708730
Gene: SLC26A2 HGNC NCBI

Linked Data

dbSNP Id: rs1044122373
gnomAD v3: 5-149981358-T-G
gnomAD v4: 5-149981358-T-G
MyVariant Identifiers: chr5:g.149360921T>G (hg19) chr5:g.149981358T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149981358T>G , CM000667.2:g.149981358T>G GRCh38
NC_000005.9:g.149360921T>G , CM000667.1:g.149360921T>G GRCh37
NC_000005.8:g.149341114T>G NCBI36
NG_007147.2:g.22476T>G , LRG_684:g.22476T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000286298.5:c.1765T>G MANE Select ENSP00000286298.4:p.Tyr589Asp
ENST00000286298.4:c.1765T>G ENSP00000286298.4:p.Tyr589Asp
ENST00000503336.1:c.372+3007T>G ENSP00000426053.1:n.372+3007T>G
NM_000112.3:c.1765T>G , LRG_684t1:c.1765T>G NP_000103.2:p.Tyr589Asp
XM_017009191.2:c.1765T>G XP_016864680.1:p.Tyr589Asp
NM_000112.4:c.1765T>G MANE Select NP_000103.2:p.Tyr589Asp
Search 100 bp 5'
Search 100 bp 3'