Canonical Allele Identifier: CA1665449792
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.134398908A= , CM000668.2:g.134398908A= GRCh38
NC_000006.11:g.134720046A= , CM000668.1:g.134720046A= GRCh37
NC_000006.10:g.134761739A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_428023.2:n.23+179A=