Canonical Allele Identifier: CA447402975

Gene: SLC26A2

Linked Data

• MyVariant Identifiers: chr5:g.149361145G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149981582G>T , CM000667.2:g.149981582G>T	GRCh38
NC_000005.9:g.149361145G>T , CM000667.1:g.149361145G>T	GRCh37
NC_000005.8:g.149341338G>T	NCBI36
NG_007147.2:g.22700G>T , LRG_684:g.22700G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286298.5:c.1989G>T MANE Select	ENSP00000286298.4:p.Gly663=
ENST00000286298.4:c.1989G>T	ENSP00000286298.4:p.Gly663=
ENST00000503336.1:c.372+3231G>T	ENSP00000426053.1:n.372+3231G>T
NM_000112.3:c.1989G>T , LRG_684t1:c.1989G>T	NP_000103.2:p.Gly663=
XM_017009191.2:c.1989G>T	XP_016864680.1:p.Gly663=
NM_000112.4:c.1989G>T MANE Select	NP_000103.2:p.Gly663=