Canonical Allele Identifier: CA1468682058
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.74553977A= , CM000666.2:g.74553977A= GRCh38
NC_000004.11:g.75419694A= , CM000666.1:g.75419694A= GRCh37

Transcript Alleles

HGVS Amino-acid change
XR_001741513.1:n.167-1145T=