Canonical Allele Identifier: CA1665449760
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.134398830T= , CM000668.2:g.134398830T= GRCh38
NC_000006.11:g.134719968T= , CM000668.1:g.134719968T= GRCh37
NC_000006.10:g.134761661T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_428023.2:n.23+101T=