Canonical Allele Identifier: CA778454136

Gene:

Linked Data

• dbSNP Id: rs1231852687
• gnomAD v3: 18-31756438-TACCC-T
• gnomAD v4: 18-31756438-TACCC-T
• MyVariant Identifiers: chr18:g.29336402_29336405del (hg19) ; chr18:g.31756439_31756442del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31756439_31756442del , CM000680.2:g.31756439_31756442del	GRCh38
NC_000018.9:g.29336402_29336405del , CM000680.1:g.29336402_29336405del	GRCh37
NC_000018.8:g.27590400_27590403del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_935338.1:n.66-5700_66-5697del