Canonical Allele Identifier: CA2492528169
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.18953470A= , CM000664.2:g.18953470A= GRCh38
NC_000002.11:g.19134748A= , CM000664.1:g.19134748A= GRCh37
NC_000002.10:g.18998229A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939775.1:n.555+9568A=