Canonical Allele Identifier: CA423314354
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2758639
ClinVar RCV Id: RCV003569799
MyVariant Identifiers: chr1:g.215901375C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215728033C>T , CM000663.2:g.215728033C>T GRCh38
NC_000001.10:g.215901375C>T , CM000663.1:g.215901375C>T GRCh37
NC_000001.9:g.213967998C>T NCBI36
NG_009497.1:g.700364G>A
NG_009497.2:g.700416G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.12063G>A MANE Select ENSP00000305941.3:p.Val4021=
ENST00000674083.1:c.12063G>A ENSP00000501296.1:p.Val4021=
ENST00000307340.7:c.12063G>A ENSP00000305941.3:p.Val4021=
NM_206933.2:c.12063G>A NP_996816.2:p.Val4021=
NM_206933.3:c.12063G>A NP_996816.2:p.Val4021=
NM_206933.4:c.12063G>A MANE Select NP_996816.3:p.Val4021=