Canonical Allele Identifier: CA168906790
Gene:

Linked Data

dbSNP Id: rs139310973
gnomAD v2: 7-148257853-GA-G
gnomAD v3: 7-148560761-GA-G
gnomAD v4: 7-148560761-GA-G
MyVariant Identifiers: chr7:g.148257854del (hg19) chr7:g.148560762del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.148560771del , CM000669.2:g.148560771del GRCh38
NC_000007.13:g.148257863del , CM000669.1:g.148257863del GRCh37
NC_000007.12:g.147888796del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928099.1:n.300+7338del
XR_928100.1:n.433+7338del
Search 100 bp 5'
Search 100 bp 3'