Canonical Allele Identifier: CA1610684931
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.11943627_11943628delinsCT , CM000668.2:g.11943627_11943628delinsCT GRCh38
NC_000006.11:g.11943860_11943861delinsCT , CM000668.1:g.11943860_11943861delinsCT GRCh37
NC_000006.10:g.12051846_12051847delinsCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001743976.1:n.348-7908_348-7907delinsCT