Canonical Allele Identifier: CA1502599208
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148649535A= , CM000666.2:g.148649535A= GRCh38
NC_000004.11:g.149570687A= , CM000666.1:g.149570687A= GRCh37
NC_000004.10:g.149790137A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939336.1:n.437-30667T=
XR_001741441.1:n.1745+104951A=
XR_939336.3:n.2921-30667T=