Canonical Allele Identifier: CA861674040

Gene:

Linked Data

• dbSNP Id: rs1477610370
• MyVariant Identifiers: chr9:g.1787475_1787477del (hg19) ; chr9:g.1787475_1787477del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.1787478_1787480del , CM000671.2:g.1787478_1787480del	GRCh38
NC_000009.11:g.1787478_1787480del , CM000671.1:g.1787478_1787480del	GRCh37
NC_000009.10:g.1777478_1777480del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001746599.1:n.142+68566_142+68568del