Canonical Allele Identifier: CA2047190485
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76004931G= , CM000674.2:g.76004931G= GRCh38
NC_000012.11:g.76398711G= , CM000674.1:g.76398711G= GRCh37
NC_000012.10:g.74684978G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945110.1:n.311+1258C=
XR_001749218.2:n.402+1258C=
XR_945110.3:n.402+1258C=