Canonical Allele Identifier: CA134548264

Gene:

Linked Data

• dbSNP Id: rs997061711
• MyVariant Identifiers: chr6:g.8169805del (hg19) ; chr6:g.8169572del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.8169576del , CM000668.2:g.8169576del	GRCh38
NC_000006.11:g.8169809del , CM000668.1:g.8169809del	GRCh37
NC_000006.10:g.8114808del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_926440.1:n.82+11316del
XR_926441.1:n.189+1656del
XR_926442.1:n.82+11316del
XR_926443.1:n.82+11316del
XR_001743950.1:n.179+1656del
XR_926440.2:n.74+11316del
XR_926441.2:n.179+1656del
XR_926443.2:n.83+11316del