Canonical Allele Identifier: CA730295495
Gene:

Linked Data

dbSNP Id: rs1355313431
MyVariant Identifiers: chr1:g.1967790C>A (hg19) chr1:g.2036351C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2036351C>A , CM000663.2:g.2036351C>A GRCh38
NC_000001.10:g.1967790C>A , CM000663.1:g.1967790C>A GRCh37
NC_000001.9:g.1957650C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_946823.1:n.773+84G>T
XR_001737845.2:n.860G>T
XR_946823.3:n.776+84G>T
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