Canonical Allele Identifier: CA1795570395
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.77413666A= , CM000670.2:g.77413666A= GRCh38
NC_000008.10:g.78325902A= , CM000670.1:g.78325902A= GRCh37
NC_000008.9:g.78488457A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929071.1:n.231-5012A=
XR_001745963.1:n.191-5012A=