Canonical Allele Identifier: CA460228569
Gene:

Linked Data

MyVariant Identifiers: chr8:g.31034235T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.31176719T>A , CM000670.2:g.31176719T>A GRCh38
NC_000008.10:g.31034235T>A , CM000670.1:g.31034235T>A GRCh37
NC_000008.9:g.31153777T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949642.1:n.271-23T>A
XR_949643.1:n.60A>T
XR_949644.1:n.60A>T
XR_949645.1:n.60A>T
XR_949646.1:n.60A>T
XR_949647.1:n.673A>T
XR_949648.1:n.575A>T
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