Canonical Allele Identifier: CA881625596
Gene:

Linked Data

dbSNP Id: rs1414534651
MyVariant Identifiers: chr19:g.34013020G>T (hg19) chr19:g.33522114G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33522114G>T , CM000681.2:g.33522114G>T GRCh38
NC_000019.9:g.34013020G>T , CM000681.1:g.34013020G>T GRCh37
NC_000019.8:g.38704860G>T NCBI36
NG_013358.1:g.4780C>A
NG_013358.2:g.4780C>A

Transcript Alleles

HGVS Amino-acid Change
XR_935918.1:n.73+100G>T
XR_935919.1:n.72+96G>T
XR_001754035.2:n.81+100G>T
XR_935918.2:n.81+100G>T
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