Canonical Allele Identifier: CA1896450371
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.23080492C= , CM000672.2:g.23080492C= GRCh38
NC_000010.10:g.23369421C= , CM000672.1:g.23369421C= GRCh37
NC_000010.9:g.23409427C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001747394.1:n.461-10924G=