Canonical Allele Identifier: CA10610218
Gene: CLDN19 HGNC NCBI

Linked Data

ClinVar Variation Id: 297322
ClinVar RCV Id: RCV000398789
dbSNP Id: rs745884385
gnomAD v2: 1-43199404-C-T
gnomAD v3: 1-42733733-C-T
gnomAD v4: 1-42733733-C-T
MyVariant Identifiers: chr1:g.43199404C>T (hg19) chr1:g.42733733C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42733733C>T , CM000663.2:g.42733733C>T GRCh38
NC_000001.10:g.43199404C>T , CM000663.1:g.43199404C>T GRCh37
NC_000001.9:g.42971991C>T NCBI36
NG_008993.1:g.11522G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000296387.6:c.*1353G>A MANE Select ENSP00000296387.1:n.*1353G>A
ENST00000296387.5:c.*1353G>A ENSP00000296387.1:n.*1353G>A
ENST00000539749.5:c.*2029G>A ENSP00000443229.1:n.*2029G>A
NM_001123395.1:c.*2135G>A NP_001116867.1:n.*2135G>A
NM_001185117.1:c.*2029G>A NP_001172046.1:n.*2029G>A
NM_148960.2:c.*1353G>A NP_683763.2:n.*1353G>A
NM_001123395.2:c.*2135G>A NP_001116867.1:n.*2135G>A
NM_148960.3:c.*1353G>A MANE Select NP_683763.2:n.*1353G>A
NM_001185117.2:c.*2029G>A NP_001172046.1:n.*2029G>A
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