Canonical Allele Identifier: CA1610684749

Gene:

Linked Data

• dbSNP Id: rs1766139925

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.11943389_11943390del , CM000668.2:g.11943389_11943390del	GRCh38
NC_000006.11:g.11943622_11943623del , CM000668.1:g.11943622_11943623del	GRCh37
NC_000006.10:g.12051608_12051609del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001743976.1:n.348-8146_348-8145del