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UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
CA16621590
Gene: USH2A
HGNC
NCBI
Linked Data
ClinVar Variation Id:
424934
ClinVar RCV Id:
RCV000488256
RCV000667007
RCV001834579
dbSNP Id:
rs1064797134
gnomAD v3:
1-215878800-C-T
gnomAD v4:
1-215878800-C-T
MyVariant Identifiers:
chr1:g.216052142C>T (hg19)
chr1:g.215878800C>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.215878800C>T , CM000663.2:g.215878800C>T
GRCh38
NC_000001.10:g.216052142C>T , CM000663.1:g.216052142C>T
GRCh37
NC_000001.9:g.214118765C>T
NCBI36
NG_009497.1:g.549597G>A
NG_009497.2:g.549649G>A
Transcript Alleles
HGVS
Amino-acid change
ENST00000307340.8:c.8522G>A
MANE Select
ENSP00000305941.3:p.Trp2841Ter
ENST00000674083.1:c.8522G>A
ENSP00000501296.1:p.Trp2841Ter
ENST00000307340.7:c.8522G>A
ENSP00000305941.3:p.Trp2841Ter
NM_206933.2:c.8522G>A
NP_996816.2:p.Trp2841Ter
NM_206933.3:c.8522G>A
NP_996816.2:p.Trp2841Ter
NM_206933.4:c.8522G>A
MANE Select
NP_996816.3:p.Trp2841Ter
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