Canonical Allele Identifier: CA307576064
Gene:

Linked Data

dbSNP Id: rs367956464
MyVariant Identifiers: chr19:g.34013023C>G (hg19) chr19:g.33522117C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33522117C>G , CM000681.2:g.33522117C>G GRCh38
NC_000019.9:g.34013023C>G , CM000681.1:g.34013023C>G GRCh37
NC_000019.8:g.38704863C>G NCBI36
NG_013358.1:g.4777G>C
NG_013358.2:g.4777G>C

Transcript Alleles

HGVS Amino-acid Change
XR_935918.1:n.73+103C>G
XR_935919.1:n.72+99C>G
XR_001754035.2:n.81+103C>G
XR_935918.2:n.81+103C>G
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