Canonical Allele Identifier: CA1144859185
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215780066A= , CM000663.2:g.215780066A= GRCh38
NC_000001.10:g.215953408A= , CM000663.1:g.215953408A= GRCh37
NC_000001.9:g.214020031A= NCBI36
NG_009497.1:g.648331T=
NG_009497.2:g.648383T=

Transcript Alleles

HGVS Amino-acid change
ENST00000307340.8:c.10741-25T= MANE Select ENSP00000305941.3:n.10741-25T=
ENST00000674083.1:c.10741-25T= ENSP00000501296.1:n.10741-25T=
ENST00000307340.7:c.10741-25T= ENSP00000305941.3:n.10741-25T=
NM_206933.2:c.10741-25T= NP_996816.2:n.10741-25T=
NM_206933.3:c.10741-25T= NP_996816.2:n.10741-25T=
NM_206933.4:c.10741-25T= MANE Select NP_996816.3:n.10741-25T=