Canonical Allele Identifier: CA361705052
Gene: SLC26A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.149357679G>C (hg19) chr5:g.149978116G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149978116G>C , CM000667.2:g.149978116G>C GRCh38
NC_000005.9:g.149357679G>C , CM000667.1:g.149357679G>C GRCh37
NC_000005.8:g.149337872G>C NCBI36
NG_007147.2:g.19234G>C , LRG_684:g.19234G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000690410.1:n.696G>C
ENST00000286298.5:c.464G>C MANE Select ENSP00000286298.4:p.Gly155Ala
ENST00000286298.4:c.464G>C ENSP00000286298.4:p.Gly155Ala
ENST00000503336.1:c.137G>C ENSP00000426053.1:p.Gly46Ala
NM_000112.3:c.464G>C , LRG_684t1:c.464G>C NP_000103.2:p.Gly155Ala
XM_017009191.2:c.464G>C XP_016864680.1:p.Gly155Ala
NM_000112.4:c.464G>C MANE Select NP_000103.2:p.Gly155Ala
Search 100 bp 5'
Search 100 bp 3'