Canonical Allele Identifier: CA2715577795
Gene: SLC26A4 HGNC NCBI

Linked Data

dbSNP Id: rs2129317230
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107696404G>A , CM000669.2:g.107696404G>A GRCh38
NC_000007.13:g.107336849G>A , CM000669.1:g.107336849G>A GRCh37
NC_000007.12:g.107124085G>A NCBI36
NG_008489.1:g.40770G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.1544+365G>A MANE Select ENSP00000494017.1:n.1544+365G>A
ENST00000644846.1:c.255+365G>A
ENST00000265715.7:c.1544+365G>A ENSP00000265715.3:n.1544+365G>A
ENST00000477350.5:n.391+365G>A
ENST00000480841.5:n.393+365G>A
NM_000441.1:c.1544+365G>A NP_000432.1:n.1544+365G>A
XM_005250425.1:c.1544+365G>A XP_005250482.1:n.1544+365G>A
XM_005250425.2:c.1544+365G>A XP_005250482.1:n.1544+365G>A
XM_017012318.1:c.1466+365G>A XP_016867807.1:n.1466+365G>A
NM_000441.2:c.1544+365G>A MANE Select NP_000432.1:n.1544+365G>A
Search 100 bp 5'
Search 100 bp 3'