Canonical Allele Identifier: CA1775343132
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.33808314T= , CM000670.2:g.33808314T= GRCh38
NC_000008.10:g.33665832T= , CM000670.1:g.33665832T= GRCh37
NC_000008.9:g.33785374T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949659.1:n.240+11878T=
XR_002956701.1:n.240+11878T=