Canonical Allele Identifier: CA1320446195
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.200033267T= , CM000664.2:g.200033267T= GRCh38
NC_000002.11:g.200897990T= , CM000664.1:g.200897990T= GRCh37
NC_000002.10:g.200606235T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923778.1:n.178-22371A=