Canonical Allele Identifier: CA1665449802

Gene:

Linked Data

• dbSNP Id: rs1774561066

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.134398929_134398931del , CM000668.2:g.134398929_134398931del	GRCh38
NC_000006.11:g.134720067_134720069del , CM000668.1:g.134720067_134720069del	GRCh37
NC_000006.10:g.134761760_134761762del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_428023.2:n.23+200_23+202del