Canonical Allele Identifier: CA344827826
Gene: USH2A HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.215813969T>C (hg19) chr1:g.215640627T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215640627T>C , CM000663.2:g.215640627T>C GRCh38
NC_000001.10:g.215813969T>C , CM000663.1:g.215813969T>C GRCh37
NC_000001.9:g.213880592T>C NCBI36
NG_009497.1:g.787770A>G
NG_009497.2:g.787822A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.14899A>G MANE Select ENSP00000305941.3:p.Thr4967Ala
ENST00000674083.1:c.14899A>G ENSP00000501296.1:p.Thr4967Ala
ENST00000307340.7:c.14899A>G ENSP00000305941.3:p.Thr4967Ala
NM_206933.2:c.14899A>G NP_996816.2:p.Thr4967Ala
NM_206933.3:c.14899A>G NP_996816.2:p.Thr4967Ala
NM_206933.4:c.14899A>G MANE Select NP_996816.3:p.Thr4967Ala
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