Canonical Allele Identifier: CA831168604

Gene: SLC26A4

Linked Data

• dbSNP Id: rs1261500003
• gnomAD v3: 7-107701040-G-T
• gnomAD v4: 7-107701040-G-T
• MyVariant Identifiers: chr7:g.107341485G>T (hg19) ; chr7:g.107701040G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107701040G>T , CM000669.2:g.107701040G>T	GRCh38
NC_000007.13:g.107341485G>T , CM000669.1:g.107341485G>T	GRCh37
NC_000007.12:g.107128721G>T	NCBI36
NG_008489.1:g.45406G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.1708-61G>T MANE Select	ENSP00000494017.1:n.1708-61G>T
ENST00000644846.1:c.419-61G>T
ENST00000265715.7:c.1708-61G>T	ENSP00000265715.3:n.1708-61G>T
ENST00000480841.5:n.557-61G>T
ENST00000492030.2:n.91-787G>T
NM_000441.1:c.1708-61G>T	NP_000432.1:n.1708-61G>T
XM_005250425.1:c.1708-61G>T	XP_005250482.1:n.1708-61G>T
XM_005250425.2:c.1708-61G>T	XP_005250482.1:n.1708-61G>T
XM_017012318.1:c.1630-61G>T	XP_016867807.1:n.1630-61G>T
NM_000441.2:c.1708-61G>T MANE Select	NP_000432.1:n.1708-61G>T