Canonical Allele Identifier: CA1247519056
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.41534565C= , CM000664.2:g.41534565C= GRCh38
NC_000002.11:g.41761705C= , CM000664.1:g.41761705C= GRCh37
NC_000002.10:g.41615209C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939996.1:n.181+3161G=
XR_939997.1:n.146+3161G=
XR_939997.2:n.9529+3161G=