Canonical Allele Identifier: CA361704003
Gene: SLC26A2 HGNC NCBI

Linked Data

dbSNP Id: rs1755017593
MyVariant Identifiers: chr5:g.149357322G>A (hg19) chr5:g.149977759G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149977759G>A , CM000667.2:g.149977759G>A GRCh38
NC_000005.9:g.149357322G>A , CM000667.1:g.149357322G>A GRCh37
NC_000005.8:g.149337515G>A NCBI36
NG_007147.2:g.18877G>A , LRG_684:g.18877G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000690410.1:n.339G>A
ENST00000286298.5:c.107G>A MANE Select ENSP00000286298.4:p.Ser36Asn
ENST00000286298.4:c.107G>A ENSP00000286298.4:p.Ser36Asn
NM_000112.3:c.107G>A , LRG_684t1:c.107G>A NP_000103.2:p.Ser36Asn
XM_017009191.2:c.107G>A XP_016864680.1:p.Ser36Asn
NM_000112.4:c.107G>A MANE Select NP_000103.2:p.Ser36Asn
Search 100 bp 5'
Search 100 bp 3'