Canonical Allele Identifier: CA2650501411
Gene: USH2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.216324145T>C , CM000663.2:g.216324145T>C GRCh38
NC_000001.10:g.216497487T>C , CM000663.1:g.216497487T>C GRCh37
NC_000001.9:g.214564110T>C NCBI36
NG_009497.1:g.104252A>G
NG_009497.2:g.104304A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000307340.8:c.1328+23A>G MANE Select ENSP00000305941.3:n.1328+23A>G
ENST00000674083.1:c.1328+23A>G ENSP00000501296.1:n.1328+23A>G
ENST00000307340.7:c.1328+23A>G ENSP00000305941.3:n.1328+23A>G
ENST00000366942.3:c.1328+23A>G ENSP00000355909.3:n.1328+23A>G
NM_007123.5:c.1328+23A>G NP_009054.5:n.1328+23A>G
NM_206933.2:c.1328+23A>G NP_996816.2:n.1328+23A>G
NM_206933.3:c.1328+23A>G NP_996816.2:n.1328+23A>G
NM_007123.6:c.1328+23A>G NP_009054.6:n.1328+23A>G
NM_206933.4:c.1328+23A>G MANE Select NP_996816.3:n.1328+23A>G