Canonical Allele Identifier: CA1757932372
Gene:

Linked Data

dbSNP Id: rs1799456378

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2180499A>G , CM000670.2:g.2180499A>G GRCh38
NC_000008.9:g.2116109A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_941356.1:n.112-12436A>G
XR_941355.2:n.133-3525A>G
XR_941356.2:n.133-12436A>G