Canonical Allele Identifier: CA20757600
Gene:

Linked Data

dbSNP Id: rs760509248
MyVariant Identifiers: chr1:g.34989150A>G (hg19) chr1:g.34523549A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34523549A>G , CM000663.2:g.34523549A>G GRCh38
NC_000001.10:g.34989150A>G , CM000663.1:g.34989150A>G GRCh37
NC_000001.9:g.34761737A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_947171.1:n.1073+24030T>C
XR_001737964.1:n.991+24030T>C
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