Canonical Allele Identifier: CA658821622
Gene:

Linked Data

ClinVar Variation Id: 554534
ClinVar RCV Id: RCV000670191
dbSNP Id: rs1554651593
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35658072_35658075delinsTGG , CM000671.2:g.35658072_35658075delinsTGG GRCh38
NC_000009.11:g.35658069_35658072delinsTGG , CM000671.1:g.35658069_35658072delinsTGG GRCh37
NC_000009.10:g.35648069_35648072delinsTGG NCBI36
NG_017041.1:g.4944_4947delinsCCA , LRG_163:g.4944_4947delinsCCA
NG_033120.1:g.4783_4786delinsTGG
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