Canonical Allele Identifier: CA2675943698

Gene: SLC26A2

Linked Data

• gnomAD v4: 5-149981882-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149981882C>T , CM000667.2:g.149981882C>T	GRCh38
NC_000005.9:g.149361445C>T , CM000667.1:g.149361445C>T	GRCh37
NC_000005.8:g.149341638C>T	NCBI36
NG_007147.2:g.23000C>T , LRG_684:g.23000C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286298.5:c.*69C>T MANE Select	ENSP00000286298.4:n.*69C>T
ENST00000286298.4:c.*69C>T	ENSP00000286298.4:n.*69C>T
ENST00000503336.1:c.372+3531C>T	ENSP00000426053.1:n.372+3531C>T
NM_000112.3:c.*69C>T , LRG_684t1:c.*69C>T	NP_000103.2:n.*69C>T
XM_017009191.2:c.*13-47C>T	XP_016864680.1:n.*13-47C>T
NM_000112.4:c.*69C>T MANE Select	NP_000103.2:n.*69C>T