Canonical Allele Identifier: CA20757647
Gene:

Linked Data

dbSNP Id: rs867415158
MyVariant Identifiers: chr1:g.34989201C>G (hg19) chr1:g.34523600C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34523600C>G , CM000663.2:g.34523600C>G GRCh38
NC_000001.10:g.34989201C>G , CM000663.1:g.34989201C>G GRCh37
NC_000001.9:g.34761788C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_947171.1:n.1073+23979G>C
XR_001737964.1:n.991+23979G>C
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