Canonical Allele Identifier: CA2284239352
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10321259C= , CM000680.2:g.10321259C= GRCh38
NC_000018.9:g.10321256C= , CM000680.1:g.10321256C= GRCh37
NC_000018.8:g.10311256C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935138.1:n.665+889G=
XR_001753344.1:n.650+889G=
XR_001753345.1:n.862G=
XR_001753346.1:n.549+889G=