Canonical Allele Identifier: CA344850954
Gene: USH2A HGNC NCBI

Linked Data

dbSNP Id: rs1657991784

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215675489G>A , CM000663.2:g.215675489G>A GRCh38
NC_000001.10:g.215848831G>A , CM000663.1:g.215848831G>A GRCh37
NC_000001.9:g.213915454G>A NCBI36
NG_009497.1:g.752908C>T
NG_009497.2:g.752960C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.12422C>T MANE Select ENSP00000305941.3:p.Ala4141Val
ENST00000674083.1:c.12422C>T ENSP00000501296.1:p.Ala4141Val
ENST00000307340.7:c.12422C>T ENSP00000305941.3:p.Ala4141Val
NM_206933.2:c.12422C>T NP_996816.2:p.Ala4141Val
NM_206933.3:c.12422C>T NP_996816.2:p.Ala4141Val
NM_206933.4:c.12422C>T MANE Select NP_996816.3:p.Ala4141Val