Canonical Allele Identifier: CA2336565999
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41648249G= , CM000681.2:g.41648249G= GRCh38
NC_000019.9:g.42152170G= , CM000681.1:g.42152170G= GRCh37
NC_000019.8:g.46844010G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935972.1:n.170+3253C=