Canonical Allele Identifier: CA361709273
Gene: SLC26A2 HGNC NCBI

Linked Data

dbSNP Id: rs373634748

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149981490G>C , CM000667.2:g.149981490G>C GRCh38
NC_000005.9:g.149361053G>C , CM000667.1:g.149361053G>C GRCh37
NC_000005.8:g.149341246G>C NCBI36
NG_007147.2:g.22608G>C , LRG_684:g.22608G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000286298.5:c.1897G>C MANE Select ENSP00000286298.4:p.Asp633His
ENST00000286298.4:c.1897G>C ENSP00000286298.4:p.Asp633His
ENST00000503336.1:c.372+3139G>C ENSP00000426053.1:n.372+3139G>C
NM_000112.3:c.1897G>C , LRG_684t1:c.1897G>C NP_000103.2:p.Asp633His
XM_017009191.2:c.1897G>C XP_016864680.1:p.Asp633His
NM_000112.4:c.1897G>C MANE Select NP_000103.2:p.Asp633His