Canonical Allele Identifier: CA164227899

Gene: SLC26A4

Linked Data

• dbSNP Id: rs571402484
• gnomAD v2: 7-107350407-C-G
• gnomAD v3: 7-107709962-C-G
• gnomAD v4: 7-107709962-C-G
• MyVariant Identifiers: chr7:g.107350407C>G (hg19) ; chr7:g.107709962C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107709962C>G , CM000669.2:g.107709962C>G	GRCh38
NC_000007.13:g.107350407C>G , CM000669.1:g.107350407C>G	GRCh37
NC_000007.12:g.107137643C>G	NCBI36
NG_008489.1:g.54328C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.2090-92C>G MANE Select	ENSP00000494017.1:n.2090-92C>G
ENST00000644846.1:c.746-92C>G
ENST00000265715.7:c.2090-92C>G	ENSP00000265715.3:n.2090-92C>G
ENST00000492030.2:n.377-193C>G
NM_000441.1:c.2090-92C>G	NP_000432.1:n.2090-92C>G
XM_005250425.1:c.2090-92C>G	XP_005250482.1:n.2090-92C>G
XM_005250425.2:c.2090-92C>G	XP_005250482.1:n.2090-92C>G
XM_017012318.1:c.2012-92C>G	XP_016867807.1:n.2012-92C>G
NM_000441.2:c.2090-92C>G MANE Select	NP_000432.1:n.2090-92C>G