Canonical Allele Identifier: CA778454350

Gene:

Linked Data

• dbSNP Id: rs1421283542
• gnomAD v3: 18-31756997-ATTTC-A
• gnomAD v4: 18-31756997-ATTTC-A
• MyVariant Identifiers: chr18:g.29336961_29336964del (hg19) ; chr18:g.31756998_31757001del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31757001_31757004del , CM000680.2:g.31757001_31757004del	GRCh38
NC_000018.9:g.29336964_29336967del , CM000680.1:g.29336964_29336967del	GRCh37
NC_000018.8:g.27590962_27590965del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_935338.1:n.66-5138_66-5135del