Canonical Allele Identifier: CA834982474
Gene:

Linked Data

dbSNP Id: rs1437747629
gnomAD v3: 7-148560929-TA-T
gnomAD v4: 7-148560929-TA-T
MyVariant Identifiers: chr7:g.148258022del (hg19) chr7:g.148560930del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.148560931del , CM000669.2:g.148560931del GRCh38
NC_000007.13:g.148258023del , CM000669.1:g.148258023del GRCh37
NC_000007.12:g.147888956del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928099.1:n.300+7170del
XR_928100.1:n.433+7170del
Search 100 bp 5'
Search 100 bp 3'