Canonical Allele Identifier: CA1305906741
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.168260451T= , CM000664.2:g.168260451T= GRCh38
NC_000002.11:g.169116961T= , CM000664.1:g.169116961T= GRCh37
NC_000002.10:g.168825207T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001739763.1:n.912-4645T=
XR_001739764.1:n.318-4645T=
XR_001739765.1:n.436-4645T=