Canonical Allele Identifier: CA817908464

Gene:

Linked Data

• dbSNP Id: rs1451803227
• MyVariant Identifiers: chr6:g.11943701_11943702del (hg19) ; chr6:g.11943468_11943469del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.11943472_11943473del , CM000668.2:g.11943472_11943473del	GRCh38
NC_000006.11:g.11943705_11943706del , CM000668.1:g.11943705_11943706del	GRCh37
NC_000006.10:g.12051691_12051692del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001743976.1:n.348-8063_348-8062del