Canonical Allele Identifier: CA1220434297
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215817009A= , CM000663.2:g.215817009A= GRCh38
NC_000001.10:g.215990351A= , CM000663.1:g.215990351A= GRCh37
NC_000001.9:g.214056974A= NCBI36
NG_009497.1:g.611388T=
NG_009497.2:g.611440T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.9558T= MANE Select ENSP00000305941.3:p.Ser3186=
ENST00000674083.1:c.9558T= ENSP00000501296.1:p.Ser3186=
ENST00000307340.7:c.9558T= ENSP00000305941.3:p.Ser3186=
NM_206933.2:c.9558T= NP_996816.2:p.Ser3186=
NM_206933.3:c.9558T= NP_996816.2:p.Ser3186=
NM_206933.4:c.9558T= MANE Select NP_996816.3:p.Ser3186=