Canonical Allele Identifier: CA447402054

Gene: SLC26A2

Linked Data

• gnomAD v4: 5-149978183-C-T
• MyVariant Identifiers: chr5:g.149357746C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149978183C>T , CM000667.2:g.149978183C>T	GRCh38
NC_000005.9:g.149357746C>T , CM000667.1:g.149357746C>T	GRCh37
NC_000005.8:g.149337939C>T	NCBI36
NG_007147.2:g.19301C>T , LRG_684:g.19301C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690410.1:n.763C>T
ENST00000286298.5:c.531C>T MANE Select	ENSP00000286298.4:p.Asp177=
ENST00000286298.4:c.531C>T	ENSP00000286298.4:p.Asp177=
ENST00000503336.1:c.204C>T	ENSP00000426053.1:p.Asp68=
NM_000112.3:c.531C>T , LRG_684t1:c.531C>T	NP_000103.2:p.Asp177=
XM_017009191.2:c.531C>T	XP_016864680.1:p.Asp177=
NM_000112.4:c.531C>T MANE Select	NP_000103.2:p.Asp177=