Canonical Allele Identifier: CA828661867

Gene:

Linked Data

• dbSNP Id: rs1317572351
• MyVariant Identifiers: chr6:g.8169669_8169691del (hg19) ; chr6:g.8169436_8169458del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.8169438_8169460del , CM000668.2:g.8169438_8169460del	GRCh38
NC_000006.11:g.8169671_8169693del , CM000668.1:g.8169671_8169693del	GRCh37
NC_000006.10:g.8114670_8114692del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_926440.1:n.82+11178_82+11200del
XR_926441.1:n.189+1518_189+1540del
XR_926442.1:n.82+11178_82+11200del
XR_926443.1:n.82+11178_82+11200del
XR_001743950.1:n.179+1518_179+1540del
XR_926440.2:n.74+11178_74+11200del
XR_926441.2:n.179+1518_179+1540del
XR_926443.2:n.83+11178_83+11200del