Canonical Allele Identifier: CA1320446174
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.200033231G= , CM000664.2:g.200033231G= GRCh38
NC_000002.11:g.200897954G= , CM000664.1:g.200897954G= GRCh37
NC_000002.10:g.200606199G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923778.1:n.178-22335C=