Canonical Allele Identifier: CA1283487527
Gene:

Linked Data

dbSNP Id: rs1690913848

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120332115_120332116del , CM000664.2:g.120332115_120332116del GRCh38
NC_000002.11:g.121089691_121089692del , CM000664.1:g.121089691_121089692del GRCh37
NC_000002.10:g.120806161_120806162del NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011512307.1:c.141+3309_141+3310del XP_011510609.1:n.141+3309_141+3310del