Canonical Allele Identifier: CA572710289
Gene:

Linked Data

dbSNP Id: rs1477324656
gnomAD v2: 7-10706864-GC-G
gnomAD v3: 7-10667237-GC-G
gnomAD v4: 7-10667237-GC-G
MyVariant Identifiers: chr7:g.10706865del (hg19) chr7:g.10667238del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.10667238del , CM000669.2:g.10667238del GRCh38
NC_000007.13:g.10706865del , CM000669.1:g.10706865del GRCh37
NC_000007.12:g.10673390del NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_147499.1:n.64-105661del
XR_001745090.1:n.376-8058del
Search 100 bp 5'
Search 100 bp 3'