Canonical Allele Identifier: CA134173695
Gene:

Linked Data

dbSNP Id: rs924913970
gnomAD v3: 6-11943358-C-CGTT
gnomAD v4: 6-11943358-C-CGTT
MyVariant Identifiers: chr6:g.11943591_11943592insGTT (hg19) chr6:g.11943358_11943359insGTT (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.11943358_11943359insGTT , CM000668.2:g.11943358_11943359insGTT GRCh38
NC_000006.11:g.11943591_11943592insGTT , CM000668.1:g.11943591_11943592insGTT GRCh37
NC_000006.10:g.12051577_12051578insGTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001743976.1:n.348-8177_348-8176insGTT
Search 100 bp 5'
Search 100 bp 3'