Canonical Allele Identifier: CA460228727
Gene:

Linked Data

gnomAD v4: 8-31176774-A-G
MyVariant Identifiers: chr8:g.31034290A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.31176774A>G , CM000670.2:g.31176774A>G GRCh38
NC_000008.10:g.31034290A>G , CM000670.1:g.31034290A>G GRCh37
NC_000008.9:g.31153832A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949642.1:n.303A>G
XR_949643.1:n.5T>C
XR_949644.1:n.5T>C
XR_949645.1:n.5T>C
XR_949646.1:n.5T>C
XR_949647.1:n.618T>C
XR_949648.1:n.520T>C