Canonical Allele Identifier: CA1697889699
Gene:
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30897483_30897487delinsGGGCC , CM000669.2:g.30897483_30897487delinsGGGCC GRCh38
NC_000007.13:g.30937098_30937102delinsGGGCC , CM000669.1:g.30937098_30937102delinsGGGCC GRCh37
NC_000007.12:g.30903623_30903627delinsGGGCC NCBI36
NG_007475.2:g.49090_49094delinsGGGCC

Transcript Alleles

HGVS Amino-acid change
ENST00000509504.2:c.621+14490_621+14494delinsGGGCC
Search 100 bp 5'
Search 100 bp 3'