Canonical Allele Identifier: CA571557064
Gene:

Linked Data

dbSNP Id: rs1361270003
gnomAD v2: 6-161089724-TG-T
gnomAD v3: 6-160668692-TG-T
gnomAD v4: 6-160668692-TG-T
MyVariant Identifiers: chr6:g.161089725del (hg19) chr6:g.160668693del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160668695del , CM000668.2:g.160668695del GRCh38
NC_000006.11:g.161089727del , CM000668.1:g.161089727del GRCh37
NC_000006.10:g.161009717del NCBI36
NG_016147.1:g.2683del

Transcript Alleles

HGVS Amino-acid change
ENST00000452651.1:n.115-2320del
Search 100 bp 5'
Search 100 bp 3'