Canonical Allele Identifier: CA1677170005
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160668682_160668685delinsATGG , CM000668.2:g.160668682_160668685delinsATGG GRCh38
NC_000006.11:g.161089714_161089717delinsATGG , CM000668.1:g.161089714_161089717delinsATGG GRCh37
NC_000006.10:g.161009704_161009707delinsATGG NCBI36
NG_016147.1:g.2691_2694delinsCCAT

Transcript Alleles

HGVS Amino-acid change
ENST00000452651.1:n.115-2312_115-2309delinsCCAT