Canonical Allele Identifier: CA361704545
Gene: SLC26A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149977904A>C , CM000667.2:g.149977904A>C GRCh38
NC_000005.9:g.149357467A>C , CM000667.1:g.149357467A>C GRCh37
NC_000005.8:g.149337660A>C NCBI36
NG_007147.2:g.19022A>C , LRG_684:g.19022A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000690410.1:n.484A>C
ENST00000286298.5:c.252A>C MANE Select ENSP00000286298.4:p.Lys84Asn
ENST00000286298.4:c.252A>C ENSP00000286298.4:p.Lys84Asn
NM_000112.3:c.252A>C , LRG_684t1:c.252A>C NP_000103.2:p.Lys84Asn
XM_017009191.2:c.252A>C XP_016864680.1:p.Lys84Asn
NM_000112.4:c.252A>C MANE Select NP_000103.2:p.Lys84Asn