Canonical Allele Identifier: CA307576018
Gene:

Linked Data

dbSNP Id: rs886932994
gnomAD v2: 19-34012927-C-T
gnomAD v3: 19-33522021-C-T
gnomAD v4: 19-33522021-C-T
MyVariant Identifiers: chr19:g.34012927C>T (hg19) chr19:g.33522021C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33522021C>T , CM000681.2:g.33522021C>T GRCh38
NC_000019.9:g.34012927C>T , CM000681.1:g.34012927C>T GRCh37
NC_000019.8:g.38704767C>T NCBI36
NG_013358.1:g.4873G>A
NG_013358.2:g.4873G>A

Transcript Alleles

HGVS Amino-acid Change
XR_935918.1:n.73+7C>T
XR_935919.1:n.72+3C>T
XR_001754035.2:n.81+7C>T
XR_935918.2:n.81+7C>T
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