Canonical Allele Identifier: CA1035793822
Gene:

Linked Data

dbSNP Id: rs1678952016

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122369217_122369218insGGAT , CM000664.2:g.122369217_122369218insGGAT GRCh38
NC_000002.11:g.123126793_123126794insGGAT , CM000664.1:g.123126793_123126794insGGAT GRCh37
NC_000002.10:g.122843263_122843264insGGAT NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923278.1:n.556-23746_556-23745insGGAT
XR_001739684.1:n.556-23746_556-23745insGGAT