Canonical Allele Identifier: CA361704008
Gene: SLC26A2 HGNC NCBI

Linked Data

dbSNP Id: rs1165698640
gnomAD v2: 5-149357324-A-G
gnomAD v4: 5-149977761-A-G
MyVariant Identifiers: chr5:g.149357324A>G (hg19) chr5:g.149977761A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149977761A>G , CM000667.2:g.149977761A>G GRCh38
NC_000005.9:g.149357324A>G , CM000667.1:g.149357324A>G GRCh37
NC_000005.8:g.149337517A>G NCBI36
NG_007147.2:g.18879A>G , LRG_684:g.18879A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000690410.1:n.341A>G
ENST00000286298.5:c.109A>G MANE Select ENSP00000286298.4:p.Thr37Ala
ENST00000286298.4:c.109A>G ENSP00000286298.4:p.Thr37Ala
NM_000112.3:c.109A>G , LRG_684t1:c.109A>G NP_000103.2:p.Thr37Ala
XM_017009191.2:c.109A>G XP_016864680.1:p.Thr37Ala
NM_000112.4:c.109A>G MANE Select NP_000103.2:p.Thr37Ala
Search 100 bp 5'
Search 100 bp 3'