Canonical Allele Identifier: CA2336565998
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41648247C= , CM000681.2:g.41648247C= GRCh38
NC_000019.9:g.42152168C= , CM000681.1:g.42152168C= GRCh37
NC_000019.8:g.46844008C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935972.1:n.170+3255G=