Canonical Allele Identifier: CA831179147
Gene: SLC26A4 HGNC NCBI

Linked Data

dbSNP Id: rs1175323624
MyVariant Identifiers: chr7:g.107357856C>T (hg19) chr7:g.107717411C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107717411C>T , CM000669.2:g.107717411C>T GRCh38
NC_000007.13:g.107357856C>T , CM000669.1:g.107357856C>T GRCh37
NC_000007.12:g.107145092C>T NCBI36
NG_008489.1:g.61777C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.*1965C>T MANE Select ENSP00000494017.1:n.*1965C>T
ENST00000265715.7:c.*1965C>T ENSP00000265715.3:n.*1965C>T
NM_000441.1:c.*1965C>T NP_000432.1:n.*1965C>T
NM_000441.2:c.*1965C>T MANE Select NP_000432.1:n.*1965C>T
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Search 100 bp 3'