Canonical Allele Identifier: CA368843721

Gene: SLC26A4

Linked Data

• dbSNP Id: rs932637607
• MyVariant Identifiers: chr7:g.107342434C>T (hg19) ; chr7:g.107701989C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107701989C>T , CM000669.2:g.107701989C>T	GRCh38
NC_000007.13:g.107342434C>T , CM000669.1:g.107342434C>T	GRCh37
NC_000007.12:g.107129670C>T	NCBI36
NG_008489.1:g.46355C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1966C>T MANE Select	ENSP00000494017.1:p.His656Tyr
ENST00000644846.1:c.677C>T
ENST00000265715.7:c.1966C>T	ENSP00000265715.3:p.His656Tyr
ENST00000492030.2:n.253C>T
NM_000441.1:c.1966C>T	NP_000432.1:p.His656Tyr
XM_005250425.1:c.1966C>T	XP_005250482.1:p.His656Tyr
XM_005250425.2:c.1966C>T	XP_005250482.1:p.His656Tyr
XM_017012318.1:c.1888C>T	XP_016867807.1:p.His630Tyr
NM_000441.2:c.1966C>T MANE Select	NP_000432.1:p.His656Tyr