Canonical Allele Identifier: CA1163454637

Gene:

Linked Data

• dbSNP Id: rs1642175709

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.38168160_38168183del , CM000663.2:g.38168160_38168183del	GRCh38
NC_000001.10:g.38633832_38633855del , CM000663.1:g.38633832_38633855del	GRCh37
NC_000001.9:g.38406419_38406442del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_947202.1:n.175+6337_175+6360del
XR_947203.1:n.62-24845_62-24822del
XR_947204.1:n.175+6337_175+6360del
XR_947205.1:n.175+6337_175+6360del
XR_001737984.1:n.175+6337_175+6360del
XR_001737985.1:n.62-24845_62-24822del
XR_001737986.1:n.175+6337_175+6360del
XR_001737987.1:n.175+6337_175+6360del
XR_002958294.1:n.175+6337_175+6360del
XR_947205.2:n.175+6337_175+6360del