Canonical Allele Identifier: CA2043864119
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68248061T= , CM000674.2:g.68248061T= GRCh38
NC_000012.11:g.68641841T= , CM000674.1:g.68641841T= GRCh37
NC_000012.10:g.66928108T= NCBI36
NG_060763.1:g.10544A=

Transcript Alleles

HGVS Amino-acid change
XR_945055.1:n.265-16597T=
XR_002957418.1:n.281-16597T=