Canonical Allele Identifier: CA368846052

Gene: SLC26A4

Linked Data

• dbSNP Id: rs1057524176
• gnomAD v4: 7-107710170-C-G
• MyVariant Identifiers: chr7:g.107350615C>G (hg19) ; chr7:g.107710170C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107710170C>G , CM000669.2:g.107710170C>G	GRCh38
NC_000007.13:g.107350615C>G , CM000669.1:g.107350615C>G	GRCh37
NC_000007.12:g.107137851C>G	NCBI36
NG_008489.1:g.54536C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.2206C>G MANE Select	ENSP00000494017.1:p.Gln736Glu
ENST00000644846.1:c.862C>G
ENST00000265715.7:c.2206C>G	ENSP00000265715.3:p.Gln736Glu
ENST00000492030.2:n.392C>G
NM_000441.1:c.2206C>G	NP_000432.1:p.Gln736Glu
XM_005250425.1:c.2206C>G	XP_005250482.1:p.Gln736Glu
XM_005250425.2:c.2206C>G	XP_005250482.1:p.Gln736Glu
XM_017012318.1:c.2128C>G	XP_016867807.1:p.Gln710Glu
NM_000441.2:c.2206C>G MANE Select	NP_000432.1:p.Gln736Glu