Canonical Allele Identifier: CA460228701
Gene:

Linked Data

gnomAD v4: 8-31176765-G-T
MyVariant Identifiers: chr8:g.31034281G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.31176765G>T , CM000670.2:g.31176765G>T GRCh38
NC_000008.10:g.31034281G>T , CM000670.1:g.31034281G>T GRCh37
NC_000008.9:g.31153823G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949642.1:n.294G>T
XR_949643.1:n.14C>A
XR_949644.1:n.14C>A
XR_949645.1:n.14C>A
XR_949646.1:n.14C>A
XR_949647.1:n.627C>A
XR_949648.1:n.529C>A