Canonical Allele Identifier: CA825142417

Gene:

Linked Data

• dbSNP Id: rs1317640114
• MyVariant Identifiers: chr6:g.465793_465799del (hg19) ; chr6:g.465793_465799del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.465796_465802del , CM000668.2:g.465796_465802del	GRCh38
NC_000006.11:g.465796_465802del , CM000668.1:g.465796_465802del	GRCh37
NC_000006.10:g.410796_410802del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_926364.1:n.2714+12071_2714+12077del
XR_926365.1:n.2548+12071_2548+12077del
XR_001743914.1:n.482-9412_482-9406del