Canonical Allele Identifier: CA1305906742
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.168260452A= , CM000664.2:g.168260452A= GRCh38
NC_000002.11:g.169116962A= , CM000664.1:g.169116962A= GRCh37
NC_000002.10:g.168825208A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001739763.1:n.912-4644A=
XR_001739764.1:n.318-4644A=
XR_001739765.1:n.436-4644A=