Canonical Allele Identifier: CA1305906743
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.168260453T= , CM000664.2:g.168260453T= GRCh38
NC_000002.11:g.169116963T= , CM000664.1:g.169116963T= GRCh37
NC_000002.10:g.168825209T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001739763.1:n.912-4643T=
XR_001739764.1:n.318-4643T=
XR_001739765.1:n.436-4643T=