Canonical Allele Identifier: CA361704535
Gene: SLC26A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149977902A>C , CM000667.2:g.149977902A>C GRCh38
NC_000005.9:g.149357465A>C , CM000667.1:g.149357465A>C GRCh37
NC_000005.8:g.149337658A>C NCBI36
NG_007147.2:g.19020A>C , LRG_684:g.19020A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000690410.1:n.482A>C
ENST00000286298.5:c.250A>C MANE Select ENSP00000286298.4:p.Lys84Gln
ENST00000286298.4:c.250A>C ENSP00000286298.4:p.Lys84Gln
NM_000112.3:c.250A>C , LRG_684t1:c.250A>C NP_000103.2:p.Lys84Gln
XM_017009191.2:c.250A>C XP_016864680.1:p.Lys84Gln
NM_000112.4:c.250A>C MANE Select NP_000103.2:p.Lys84Gln