Canonical Allele Identifier: CA170474101
Gene:

Linked Data

dbSNP Id: rs913546245
MyVariant Identifiers: chr8:g.2180597G>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2180597G>T , CM000670.2:g.2180597G>T GRCh38
NC_000008.9:g.2116207G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_941356.1:n.112-12338G>T
XR_941355.2:n.133-3427G>T
XR_941356.2:n.133-12338G>T