Canonical Allele Identifier: CA1697889741
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30897570_30897571delinsAG , CM000669.2:g.30897570_30897571delinsAG GRCh38
NC_000007.13:g.30937185_30937186delinsAG , CM000669.1:g.30937185_30937186delinsAG GRCh37
NC_000007.12:g.30903710_30903711delinsAG NCBI36
NG_007475.2:g.49177_49178delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000509504.2:c.622-14423_622-14422delinsAG