Canonical Allele Identifier: CA607406225
Gene:

Linked Data

dbSNP Id: rs72072572
gnomAD v2: 12-102895078-CTCAATCAATCAA-C
gnomAD v3: 12-102501300-CTCAATCAATCAA-C
gnomAD v4: 12-102501300-CTCAATCAATCAA-C
MyVariant Identifiers: chr12:g.102895079_102895090del (hg19) chr12:g.102501301_102501312del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102501318_102501329del , CM000674.2:g.102501318_102501329del GRCh38
NC_000012.11:g.102895096_102895107del , CM000674.1:g.102895096_102895107del GRCh37
NC_000012.10:g.101419226_101419237del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001749289.1:n.1952+17430_1952+17441del
Search 100 bp 5'
Search 100 bp 3'