Canonical Allele Identifier: CA344825039
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 554244
ClinVar RCV Id: RCV000669839
dbSNP Id: rs1553265829
MyVariant Identifiers: chr1:g.215990456A>T (hg19) chr1:g.215817114A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215817114A>T , CM000663.2:g.215817114A>T GRCh38
NC_000001.10:g.215990456A>T , CM000663.1:g.215990456A>T GRCh37
NC_000001.9:g.214057079A>T NCBI36
NG_009497.1:g.611283T>A
NG_009497.2:g.611335T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.9453T>A MANE Select ENSP00000305941.3:p.Tyr3151Ter
ENST00000674083.1:c.9453T>A ENSP00000501296.1:p.Tyr3151Ter
ENST00000307340.7:c.9453T>A ENSP00000305941.3:p.Tyr3151Ter
NM_206933.2:c.9453T>A NP_996816.2:p.Tyr3151Ter
NM_206933.3:c.9453T>A NP_996816.2:p.Tyr3151Ter
NM_206933.4:c.9453T>A MANE Select NP_996816.3:p.Tyr3151Ter
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