Canonical Allele Identifier: CA460228530
Gene:

Linked Data

MyVariant Identifiers: chr8:g.31034221G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.31176705G>T , CM000670.2:g.31176705G>T GRCh38
NC_000008.10:g.31034221G>T , CM000670.1:g.31034221G>T GRCh37
NC_000008.9:g.31153763G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949642.1:n.271-37G>T
XR_949643.1:n.74C>A
XR_949644.1:n.74C>A
XR_949645.1:n.74C>A
XR_949646.1:n.74C>A
XR_949647.1:n.687C>A
XR_949648.1:n.589C>A
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