Canonical Allele Identifier: CA1502599189
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148649528T= , CM000666.2:g.148649528T= GRCh38
NC_000004.11:g.149570680T= , CM000666.1:g.149570680T= GRCh37
NC_000004.10:g.149790130T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939336.1:n.437-30660A=
XR_001741441.1:n.1745+104944T=
XR_939336.3:n.2921-30660A=