Canonical Allele Identifier: CA1247519052
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.41534559C= , CM000664.2:g.41534559C= GRCh38
NC_000002.11:g.41761699C= , CM000664.1:g.41761699C= GRCh37
NC_000002.10:g.41615203C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939996.1:n.181+3167G=
XR_939997.1:n.146+3167G=
XR_939997.2:n.9529+3167G=