Canonical Allele Identifier: CA2345843979
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.1875456G= , CM000682.2:g.1875456G= GRCh38
NC_000020.10:g.1856102G= , CM000682.1:g.1856102G= GRCh37
NC_000020.9:g.1804102G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001754467.1:n.433-7363C=