Canonical Allele Identifier: CA1220416560
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215782002C= , CM000663.2:g.215782002C= GRCh38
NC_000001.10:g.215955344C= , CM000663.1:g.215955344C= GRCh37
NC_000001.9:g.214021967C= NCBI36
NG_009497.1:g.646395G=
NG_009497.2:g.646447G=

Transcript Alleles

HGVS Amino-acid change
ENST00000307340.8:c.10740+40G= MANE Select ENSP00000305941.3:n.10740+40G=
ENST00000674083.1:c.10740+40G= ENSP00000501296.1:n.10740+40G=
ENST00000307340.7:c.10740+40G= ENSP00000305941.3:n.10740+40G=
NM_206933.2:c.10740+40G= NP_996816.2:n.10740+40G=
NM_206933.3:c.10740+40G= NP_996816.2:n.10740+40G=
NM_206933.4:c.10740+40G= MANE Select NP_996816.3:n.10740+40G=