Canonical Allele Identifier: CA462389084
Gene:

Linked Data

MyVariant Identifiers: chr8:g.98281759T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.97269531T>G , CM000670.2:g.97269531T>G GRCh38
NC_000008.10:g.98281759T>G , CM000670.1:g.98281759T>G GRCh37
NC_000008.9:g.98350935T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125390.1:n.471+149539A>C