Canonical Allele Identifier: CA344851244
Gene: USH2A HGNC NCBI

Linked Data

COSMIC: COSM463931 COSM4858372
MyVariant Identifiers: chr1:g.215848923G>T (hg19) chr1:g.215675581G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215675581G>T , CM000663.2:g.215675581G>T GRCh38
NC_000001.10:g.215848923G>T , CM000663.1:g.215848923G>T GRCh37
NC_000001.9:g.213915546G>T NCBI36
NG_009497.1:g.752816C>A
NG_009497.2:g.752868C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.12330C>A MANE Select ENSP00000305941.3:p.Tyr4110Ter
ENST00000674083.1:c.12330C>A ENSP00000501296.1:p.Tyr4110Ter
ENST00000307340.7:c.12330C>A ENSP00000305941.3:p.Tyr4110Ter
NM_206933.2:c.12330C>A NP_996816.2:p.Tyr4110Ter
NM_206933.3:c.12330C>A NP_996816.2:p.Tyr4110Ter
NM_206933.4:c.12330C>A MANE Select NP_996816.3:p.Tyr4110Ter
Search 100 bp 5'
Search 100 bp 3'