Canonical Allele Identifier: CA1122483663
Gene:

Linked Data

dbSNP Id: rs377685777

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551510_25551511insTGTAAAACAGCCTTTTACAGTCTTTT , CM000671.2:g.25551510_25551511insTGTAAAACAGCCTTTTACAGTCTTTT GRCh38
NC_000009.11:g.25551508_25551509insTGTAAAACAGCCTTTTACAGTCTTTT , CM000671.1:g.25551508_25551509insTGTAAAACAGCCTTTTACAGTCTTTT GRCh37
NC_000009.10:g.25541508_25541509insTGTAAAACAGCCTTTTACAGTCTTTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929525.1:n.50-939_50-938insAAAAGACTGTAAAAGGCTGTTTTACA
XR_929525.2:n.674-939_674-938insAAAAGACTGTAAAAGGCTGTTTTACA