Canonical Allele Identifier: CA344836183
Gene: USH2A HGNC NCBI

Linked Data

dbSNP Id: rs1259758261
gnomAD v2: 1-215955403-C-T
gnomAD v4: 1-215782061-C-T
MyVariant Identifiers: chr1:g.215955403C>T (hg19) chr1:g.215782061C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215782061C>T , CM000663.2:g.215782061C>T GRCh38
NC_000001.10:g.215955403C>T , CM000663.1:g.215955403C>T GRCh37
NC_000001.9:g.214022026C>T NCBI36
NG_009497.1:g.646336G>A
NG_009497.2:g.646388G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.10721G>A MANE Select ENSP00000305941.3:p.Gly3574Asp
ENST00000674083.1:c.10721G>A ENSP00000501296.1:p.Gly3574Asp
ENST00000307340.7:c.10721G>A ENSP00000305941.3:p.Gly3574Asp
NM_206933.2:c.10721G>A NP_996816.2:p.Gly3574Asp
NM_206933.3:c.10721G>A NP_996816.2:p.Gly3574Asp
NM_206933.4:c.10721G>A MANE Select NP_996816.3:p.Gly3574Asp
Search 100 bp 5'
Search 100 bp 3'