Canonical Allele Identifier: CA1601249928
Gene: SH3PXD2B HGNC NCBI

Linked Data

dbSNP Id: rs1756607981

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.172333464_172333465insAGA , CM000667.2:g.172333464_172333465insAGA GRCh38
NC_000005.9:g.171760468_171760469insAGA , CM000667.1:g.171760468_171760469insAGA GRCh37
NC_000005.8:g.171693073_171693074insAGA NCBI36
NG_027746.1:g.126059_126060insTCT
NG_027746.2:g.126059_126060insTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000636523.1:c.1229-8085_1229-8084insTCT
ENST00000519643.5:c.1189-8085_1189-8084insTCT ENSP00000430890.1:n.1189-8085_1189-8084insTCT
NM_001308175.1:c.1189-8085_1189-8084insTCT NP_001295104.1:n.1189-8085_1189-8084insTCT
NM_001308175.2:c.1189-8085_1189-8084insTCT NP_001295104.1:n.1189-8085_1189-8084insTCT