Canonical Allele Identifier: CA1605795110

Gene:

Linked Data

• dbSNP Id: rs1761320764

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.1535912_1535914del , CM000668.2:g.1535912_1535914del	GRCh38
NC_000006.11:g.1536147_1536149del , CM000668.1:g.1536147_1536149del	GRCh37
NC_000006.10:g.1481146_1481148del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_427861.2:n.234+16434_234+16436del
XR_926380.1:n.218-2544_218-2542del
XR_926381.1:n.1108-2544_1108-2542del
XR_926382.1:n.235-6733_235-6731del
XR_926384.1:n.200-6733_200-6731del
XR_001743921.1:n.235-6757_235-6755del
XR_427861.3:n.234+16434_234+16436del
XR_926381.2:n.1123-2544_1123-2542del