Canonical Allele Identifier: CA460228686
Gene:

Linked Data

gnomAD v4: 8-31176760-G-T
MyVariant Identifiers: chr8:g.31034276G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.31176760G>T , CM000670.2:g.31176760G>T GRCh38
NC_000008.10:g.31034276G>T , CM000670.1:g.31034276G>T GRCh37
NC_000008.9:g.31153818G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949642.1:n.289G>T
XR_949643.1:n.19C>A
XR_949644.1:n.19C>A
XR_949645.1:n.19C>A
XR_949646.1:n.19C>A
XR_949647.1:n.632C>A
XR_949648.1:n.534C>A