Canonical Allele Identifier: CA457105375
Gene: SLC26A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.107314682A>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107674237A>C , CM000669.2:g.107674237A>C GRCh38
NC_000007.13:g.107314682A>C , CM000669.1:g.107314682A>C GRCh37
NC_000007.12:g.107101918A>C NCBI36
NG_008489.1:g.18603A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.489A>C MANE Select ENSP00000494017.1:p.Val163=
ENST00000265715.7:c.489A>C ENSP00000265715.3:p.Val163=
NM_000441.1:c.489A>C NP_000432.1:p.Val163=
XM_005250425.1:c.489A>C XP_005250482.1:p.Val163=
XM_006716025.2:c.489A>C XP_006716088.1:p.Val163=
XM_005250425.2:c.489A>C XP_005250482.1:p.Val163=
XM_006716025.3:c.489A>C XP_006716088.1:p.Val163=
XM_017012318.1:c.489A>C XP_016867807.1:p.Val163=
NM_000441.2:c.489A>C MANE Select NP_000432.1:p.Val163=
Search 100 bp 5'
Search 100 bp 3'