Canonical Allele Identifier: CA150690511

Gene:

Linked Data

• dbSNP Id: rs371836779
• gnomAD v2: 6-156133724-TG-T
• gnomAD v3: 6-155812590-TG-T
• gnomAD v4: 6-155812590-TG-T
• MyVariant Identifiers: chr6:g.156133725del (hg19) ; chr6:g.155812591del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.155812591del , CM000668.2:g.155812591del	GRCh38
NC_000006.11:g.156133725del , CM000668.1:g.156133725del	GRCh37
NC_000006.10:g.156175417del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943142.1:n.79+19172del
XR_943146.1:n.645-552del
XR_001744423.1:n.699-552del
XR_001744424.1:n.79+19172del