Canonical Allele Identifier: CA821666551

Gene:

Linked Data

• dbSNP Id: rs1438145493
• gnomAD v3: 6-160668488-AC-A
• gnomAD v4: 6-160668488-AC-A
• MyVariant Identifiers: chr6:g.161089521del (hg19) ; chr6:g.160668489del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160668490del , CM000668.2:g.160668490del	GRCh38
NC_000006.11:g.161089522del , CM000668.1:g.161089522del	GRCh37
NC_000006.10:g.161009512del	NCBI36
NG_016147.1:g.2887del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452651.1:n.115-2116del