Canonical Allele Identifier: CA916402751
Gene: USH2A HGNC NCBI

Linked Data

dbSNP Id: rs1571679618

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215780257del , CM000663.2:g.215780257del GRCh38
NC_000001.10:g.215953599del , CM000663.1:g.215953599del GRCh37
NC_000001.9:g.214020222del NCBI36
NG_009497.1:g.648141del
NG_009497.2:g.648193del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.10741-215del MANE Select ENSP00000305941.3:n.10741-215del
ENST00000674083.1:c.10741-215del ENSP00000501296.1:n.10741-215del
ENST00000307340.7:c.10741-215del ENSP00000305941.3:n.10741-215del
NM_206933.2:c.10741-215del NP_996816.2:n.10741-215del
NM_206933.3:c.10741-215del NP_996816.2:n.10741-215del
NM_206933.4:c.10741-215del MANE Select NP_996816.3:n.10741-215del