Canonical Allele Identifier: CA1222435238
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.220491638G= , CM000663.2:g.220491638G= GRCh38
NC_000001.10:g.220664980G= , CM000663.1:g.220664980G= GRCh37
NC_000001.9:g.218731603G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_922615.1:n.256-596G=
XR_001737822.1:n.557-596G=