Canonical Allele Identifier: CA729869706
Gene:

Linked Data

dbSNP Id: rs1398120856
MyVariant Identifiers: chr1:g.20201015T>A (hg19) chr1:g.19874522T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.19874522T>A , CM000663.2:g.19874522T>A GRCh38
NC_000001.10:g.20201015T>A , CM000663.1:g.20201015T>A GRCh37
NC_000001.9:g.20073602T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_947027.1:n.266-8770A>T
XR_947028.1:n.266-8770A>T
XR_947027.2:n.167-8770A>T
XR_947028.2:n.167-8770A>T
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