Canonical Allele Identifier: CA1141733210
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215779955G= , CM000663.2:g.215779955G= GRCh38
NC_000001.10:g.215953297G= , CM000663.1:g.215953297G= GRCh37
NC_000001.9:g.214019920G= NCBI36
NG_009497.1:g.648442C=
NG_009497.2:g.648494C=

Transcript Alleles

HGVS Amino-acid change
ENST00000307340.8:c.10827C= MANE Select ENSP00000305941.3:p.Ser3609=
ENST00000674083.1:c.10827C= ENSP00000501296.1:p.Ser3609=
ENST00000307340.7:c.10827C= ENSP00000305941.3:p.Ser3609=
NM_206933.2:c.10827C= NP_996816.2:p.Ser3609=
NM_206933.3:c.10827C= NP_996816.2:p.Ser3609=
NM_206933.4:c.10827C= MANE Select NP_996816.3:p.Ser3609=