Canonical Allele Identifier: CA164215562

Gene: SLC26A4

Linked Data

• dbSNP Id: rs888813949
• gnomAD v3: 7-107696389-A-G
• gnomAD v4: 7-107696389-A-G
• MyVariant Identifiers: chr7:g.107336834A>G (hg19) ; chr7:g.107696389A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107696389A>G , CM000669.2:g.107696389A>G	GRCh38
NC_000007.13:g.107336834A>G , CM000669.1:g.107336834A>G	GRCh37
NC_000007.12:g.107124070A>G	NCBI36
NG_008489.1:g.40755A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1544+350A>G MANE Select	ENSP00000494017.1:n.1544+350A>G
ENST00000644846.1:c.255+350A>G
ENST00000265715.7:c.1544+350A>G	ENSP00000265715.3:n.1544+350A>G
ENST00000477350.5:n.391+350A>G
ENST00000480841.5:n.393+350A>G
NM_000441.1:c.1544+350A>G	NP_000432.1:n.1544+350A>G
XM_005250425.1:c.1544+350A>G	XP_005250482.1:n.1544+350A>G
XM_005250425.2:c.1544+350A>G	XP_005250482.1:n.1544+350A>G
XM_017012318.1:c.1466+350A>G	XP_016867807.1:n.1466+350A>G
NM_000441.2:c.1544+350A>G MANE Select	NP_000432.1:n.1544+350A>G