Canonical Allele Identifier: CA1665449798
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.134398922A= , CM000668.2:g.134398922A= GRCh38
NC_000006.11:g.134720060A= , CM000668.1:g.134720060A= GRCh37
NC_000006.10:g.134761753A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_428023.2:n.23+193A=