Canonical Allele Identifier: CA307576011
Gene:

Linked Data

dbSNP Id: rs939245844
MyVariant Identifiers: chr19:g.34012919C>G (hg19) chr19:g.33522013C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33522013C>G , CM000681.2:g.33522013C>G GRCh38
NC_000019.9:g.34012919C>G , CM000681.1:g.34012919C>G GRCh37
NC_000019.8:g.38704759C>G NCBI36
NG_013358.1:g.4881G>C
NG_013358.2:g.4881G>C

Transcript Alleles

HGVS Amino-acid Change
XR_935918.1:n.72C>G
XR_935919.1:n.67C>G
XR_001754035.2:n.80C>G
XR_935918.2:n.80C>G
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