Canonical Allele Identifier: CA631761643
Gene:

Linked Data

dbSNP Id: rs1568379897
gnomAD v2: 19-11071356-G-GCCT
gnomAD v3: 19-10960680-G-GCCT
gnomAD v4: 19-10960680-G-GCCT
MyVariant Identifiers: chr19:g.11071356_11071357insCCT (hg19) chr19:g.10960680_10960681insCCT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10960682_10960683insTCC , CM000681.2:g.10960682_10960683insTCC GRCh38
NC_000019.9:g.11071358_11071359insTCC , CM000681.1:g.11071358_11071359insTCC GRCh37
NC_000019.8:g.10932358_10932359insTCC NCBI36
NG_011556.2:g.4761_4762insTCC
NG_011556.3:g.4751_4752insTCC
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