Canonical Allele Identifier: CA1247519093
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.41534626T= , CM000664.2:g.41534626T= GRCh38
NC_000002.11:g.41761766T= , CM000664.1:g.41761766T= GRCh37
NC_000002.10:g.41615270T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939996.1:n.181+3100A=
XR_939997.1:n.146+3100A=
XR_939997.2:n.9529+3100A=