Canonical Allele Identifier: CA1220396663
Gene: USH2A HGNC NCBI

Linked Data

dbSNP Id: rs1659900485

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215728577T>A , CM000663.2:g.215728577T>A GRCh38
NC_000001.10:g.215901919T>A , CM000663.1:g.215901919T>A GRCh37
NC_000001.9:g.213968542T>A NCBI36
NG_009497.1:g.699820A>T
NG_009497.2:g.699872A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.11712-193A>T MANE Select ENSP00000305941.3:n.11712-193A>T
ENST00000674083.1:c.11712-193A>T ENSP00000501296.1:n.11712-193A>T
ENST00000307340.7:c.11712-193A>T ENSP00000305941.3:n.11712-193A>T
NM_206933.2:c.11712-193A>T NP_996816.2:n.11712-193A>T
NM_206933.3:c.11712-193A>T NP_996816.2:n.11712-193A>T
NM_206933.4:c.11712-193A>T MANE Select NP_996816.3:n.11712-193A>T