Canonical Allele Identifier: CA566344755

Gene:

Linked Data

• dbSNP Id: rs1465146520
• gnomAD v2: 6-31407478-TG-T
• gnomAD v3: 6-31439701-TG-T
• gnomAD v4: 6-31439701-TG-T
• MyVariant Identifiers: chr6:g.31407479del (hg19) ; chr6:g.31439702del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31439702del , CM000668.2:g.31439702del	GRCh38
NC_000006.11:g.31407479del , CM000668.1:g.31407479del	GRCh37
NC_000006.10:g.31515458del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_926694.1:n.405del