Canonical Allele Identifier: CA1220455674
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215867063T= , CM000663.2:g.215867063T= GRCh38
NC_000001.10:g.216040405T= , CM000663.1:g.216040405T= GRCh37
NC_000001.9:g.214107028T= NCBI36
NG_009497.1:g.561334A=
NG_009497.2:g.561386A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.8789A= MANE Select ENSP00000305941.3:p.Asn2930=
ENST00000674083.1:c.8789A= ENSP00000501296.1:p.Asn2930=
ENST00000307340.7:c.8789A= ENSP00000305941.3:p.Asn2930=
NM_206933.2:c.8789A= NP_996816.2:p.Asn2930=
NM_206933.3:c.8789A= NP_996816.2:p.Asn2930=
NM_206933.4:c.8789A= MANE Select NP_996816.3:p.Asn2930=