Canonical Allele Identifier: CA2336566032
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41648313A= , CM000681.2:g.41648313A= GRCh38
NC_000019.9:g.42152234A= , CM000681.1:g.42152234A= GRCh37
NC_000019.8:g.46844074A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935972.1:n.170+3189T=