Canonical Allele Identifier: CA460228693
Gene:

Linked Data

dbSNP Id: rs1804278224
gnomAD v3: 8-31176763-G-A
gnomAD v4: 8-31176763-G-A
MyVariant Identifiers: chr8:g.31034279G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.31176763G>A , CM000670.2:g.31176763G>A GRCh38
NC_000008.10:g.31034279G>A , CM000670.1:g.31034279G>A GRCh37
NC_000008.9:g.31153821G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949642.1:n.292G>A
XR_949643.1:n.16C>T
XR_949644.1:n.16C>T
XR_949645.1:n.16C>T
XR_949646.1:n.16C>T
XR_949647.1:n.629C>T
XR_949648.1:n.531C>T