Canonical Allele Identifier: CA2293960085

Gene:

Linked Data

• dbSNP Id: rs2031431380

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31756519_31756527del , CM000680.2:g.31756519_31756527del	GRCh38
NC_000018.9:g.29336482_29336490del , CM000680.1:g.29336482_29336490del	GRCh37
NC_000018.8:g.27590480_27590488del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_935338.1:n.66-5620_66-5612del