Canonical Allele Identifier: CA1267947522
Gene:

Linked Data

dbSNP Id: rs1672683338

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016313_88016314insTGTTTCCAAAA , CM000664.2:g.88016313_88016314insTGTTTCCAAAA GRCh38
NC_000002.11:g.88315832_88315833insTGTTTCCAAAA , CM000664.1:g.88315832_88315833insTGTTTCCAAAA GRCh37
NC_000002.10:g.88096947_88096948insTGTTTCCAAAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.658_659insTGTTTCCAAAA
XR_940336.3:n.658_659insTGTTTCCAAAA