Canonical Allele Identifier: CA1247518979
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.41534441T= , CM000664.2:g.41534441T= GRCh38
NC_000002.11:g.41761581T= , CM000664.1:g.41761581T= GRCh37
NC_000002.10:g.41615085T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939996.1:n.181+3285A=
XR_939997.1:n.146+3285A=
XR_939997.2:n.9529+3285A=