Canonical Allele Identifier: CA1320500232
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.200157231T= , CM000664.2:g.200157231T= GRCh38
NC_000002.11:g.201021954T= , CM000664.1:g.201021954T= GRCh37
NC_000002.10:g.200730199T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923778.1:n.177+17339A=