Canonical Allele Identifier: CA361704728
Gene: SLC26A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149977966A>G , CM000667.2:g.149977966A>G GRCh38
NC_000005.9:g.149357529A>G , CM000667.1:g.149357529A>G GRCh37
NC_000005.8:g.149337722A>G NCBI36
NG_007147.2:g.19084A>G , LRG_684:g.19084A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000690410.1:n.546A>G
ENST00000286298.5:c.314A>G MANE Select ENSP00000286298.4:p.Lys105Arg
ENST00000286298.4:c.314A>G ENSP00000286298.4:p.Lys105Arg
NM_000112.3:c.314A>G , LRG_684t1:c.314A>G NP_000103.2:p.Lys105Arg
XM_017009191.2:c.314A>G XP_016864680.1:p.Lys105Arg
NM_000112.4:c.314A>G MANE Select NP_000103.2:p.Lys105Arg