Canonical Allele Identifier: CA817908390

Gene:

Linked Data

• dbSNP Id: rs1372756903
• gnomAD v3: 6-11943327-CG-C
• gnomAD v4: 6-11943327-CG-C
• MyVariant Identifiers: chr6:g.11943561del (hg19) ; chr6:g.11943328del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.11943330del , CM000668.2:g.11943330del	GRCh38
NC_000006.11:g.11943563del , CM000668.1:g.11943563del	GRCh37
NC_000006.10:g.12051549del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001743976.1:n.348-8205del