Canonical Allele Identifier: CA54648283
Gene:

Linked Data

dbSNP Id: rs765502040

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120331966_120331968del , CM000664.2:g.120331966_120331968del GRCh38
NC_000002.11:g.121089542_121089544del , CM000664.1:g.121089542_121089544del GRCh37
NC_000002.10:g.120806012_120806014del NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011512307.1:c.141+3160_141+3162del XP_011510609.1:n.141+3160_141+3162del