Canonical Allele Identifier: CA1818149984
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999820A= , CM000670.2:g.126999820A= GRCh38
NC_000008.10:g.128012065A= , CM000670.1:g.128012065A= GRCh37
NC_000008.9:g.128081247A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746076.2:n.1301-6735A=