Canonical Allele Identifier: CA1697889702
Gene:
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30897490_30897495delinsGCCCCT , CM000669.2:g.30897490_30897495delinsGCCCCT GRCh38
NC_000007.13:g.30937105_30937110delinsGCCCCT , CM000669.1:g.30937105_30937110delinsGCCCCT GRCh37
NC_000007.12:g.30903630_30903635delinsGCCCCT NCBI36
NG_007475.2:g.49097_49102delinsGCCCCT

Transcript Alleles

HGVS Amino-acid change
ENST00000509504.2:c.621+14497_622-14498delinsGCCCCT
Search 100 bp 5'
Search 100 bp 3'