Canonical Allele Identifier: CA344829690
Gene: USH2A HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.215901688A>C (hg19) chr1:g.215728346A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215728346A>C , CM000663.2:g.215728346A>C GRCh38
NC_000001.10:g.215901688A>C , CM000663.1:g.215901688A>C GRCh37
NC_000001.9:g.213968311A>C NCBI36
NG_009497.1:g.700051T>G
NG_009497.2:g.700103T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.11750T>G MANE Select ENSP00000305941.3:p.Val3917Gly
ENST00000674083.1:c.11750T>G ENSP00000501296.1:p.Val3917Gly
ENST00000307340.7:c.11750T>G ENSP00000305941.3:p.Val3917Gly
NM_206933.2:c.11750T>G NP_996816.2:p.Val3917Gly
NM_206933.3:c.11750T>G NP_996816.2:p.Val3917Gly
NM_206933.4:c.11750T>G MANE Select NP_996816.3:p.Val3917Gly
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