Canonical Allele Identifier: CA460228713
Gene:

Linked Data

gnomAD v4: 8-31176769-G-T
MyVariant Identifiers: chr8:g.31034285G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.31176769G>T , CM000670.2:g.31176769G>T GRCh38
NC_000008.10:g.31034285G>T , CM000670.1:g.31034285G>T GRCh37
NC_000008.9:g.31153827G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949642.1:n.298G>T
XR_949643.1:n.10C>A
XR_949644.1:n.10C>A
XR_949645.1:n.10C>A
XR_949646.1:n.10C>A
XR_949647.1:n.623C>A
XR_949648.1:n.525C>A