Canonical Allele Identifier: CA460228628
Gene:

Linked Data

MyVariant Identifiers: chr8:g.31034256A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.31176740A>G , CM000670.2:g.31176740A>G GRCh38
NC_000008.10:g.31034256A>G , CM000670.1:g.31034256A>G GRCh37
NC_000008.9:g.31153798A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949642.1:n.271-2A>G
XR_949643.1:n.39T>C
XR_949644.1:n.39T>C
XR_949645.1:n.39T>C
XR_949646.1:n.39T>C
XR_949647.1:n.652T>C
XR_949648.1:n.554T>C
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