Canonical Allele Identifier: CA830285623

Gene:

Linked Data

• dbSNP Id: rs1256535187
• gnomAD v3: 6-98102487-TC-T
• gnomAD v4: 6-98102487-TC-T
• MyVariant Identifiers: chr6:g.98550364del (hg19) ; chr6:g.98102488del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98102488del , CM000668.2:g.98102488del	GRCh38
NC_000006.11:g.98550364del , CM000668.1:g.98550364del	GRCh37
NC_000006.10:g.98657085del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_245563.2:n.456+3218del
XR_942809.1:n.456+3218del