Canonical Allele Identifier: CA805532927

Gene: SLC26A2

Linked Data

• dbSNP Id: rs1401139745
• MyVariant Identifiers: chr5:g.149361467C>T (hg19) ; chr5:g.149981904C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149981904C>T , CM000667.2:g.149981904C>T	GRCh38
NC_000005.9:g.149361467C>T , CM000667.1:g.149361467C>T	GRCh37
NC_000005.8:g.149341660C>T	NCBI36
NG_007147.2:g.23022C>T , LRG_684:g.23022C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286298.5:c.*91C>T MANE Select	ENSP00000286298.4:n.*91C>T
ENST00000286298.4:c.*91C>T	ENSP00000286298.4:n.*91C>T
ENST00000503336.1:c.372+3553C>T	ENSP00000426053.1:n.372+3553C>T
NM_000112.3:c.*91C>T , LRG_684t1:c.*91C>T	NP_000103.2:n.*91C>T
XM_017009191.2:c.*13-25C>T	XP_016864680.1:n.*13-25C>T
NM_000112.4:c.*91C>T MANE Select	NP_000103.2:n.*91C>T