Canonical Allele Identifier: CA830286067

Gene:

Linked Data

• dbSNP Id: rs1443665094
• gnomAD v3: 6-98014746-TTA-T
• gnomAD v4: 6-98014746-TTA-T
• MyVariant Identifiers: chr6:g.98462623_98462624del (hg19) ; chr6:g.98014747_98014748del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98014748_98014749del , CM000668.2:g.98014748_98014749del	GRCh38
NC_000006.11:g.98462624_98462625del , CM000668.1:g.98462624_98462625del	GRCh37
NC_000006.10:g.98569345_98569346del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_245563.2:n.371+45282_371+45283del
XR_942809.1:n.371+45282_371+45283del