Canonical Allele Identifier: CA1035793844
Gene:

Linked Data

dbSNP Id: rs1678953092

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122369245_122369246insGGAT , CM000664.2:g.122369245_122369246insGGAT GRCh38
NC_000002.11:g.123126821_123126822insGGAT , CM000664.1:g.123126821_123126822insGGAT GRCh37
NC_000002.10:g.122843291_122843292insGGAT NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923278.1:n.556-23718_556-23717insGGAT
XR_001739684.1:n.556-23718_556-23717insGGAT