Canonical Allele Identifier: CA1033290865
Gene:

Linked Data

dbSNP Id: rs1672673438

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016113_88016114del , CM000664.2:g.88016113_88016114del GRCh38
NC_000002.11:g.88315632_88315633del , CM000664.1:g.88315632_88315633del GRCh37
NC_000002.10:g.88096747_88096748del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.458_459del
XR_940336.3:n.458_459del