Canonical Allele Identifier: CA3505277
Gene: SLC26A2 HGNC NCBI

Linked Data

dbSNP Id: rs760309344

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149978220A>T , CM000667.2:g.149978220A>T GRCh38
NC_000005.9:g.149357783A>T , CM000667.1:g.149357783A>T GRCh37
NC_000005.8:g.149337976A>T NCBI36
NG_007147.2:g.19338A>T , LRG_684:g.19338A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000690410.1:n.800A>T
ENST00000286298.5:c.568A>T MANE Select ENSP00000286298.4:p.Ser190Cys
ENST00000286298.4:c.568A>T ENSP00000286298.4:p.Ser190Cys
ENST00000503336.1:c.241A>T ENSP00000426053.1:p.Ser81Cys
NM_000112.3:c.568A>T , LRG_684t1:c.568A>T NP_000103.2:p.Ser190Cys
XM_017009191.2:c.568A>T XP_016864680.1:p.Ser190Cys
NM_000112.4:c.568A>T MANE Select NP_000103.2:p.Ser190Cys