Canonical Allele Identifier: CA344826917
Gene: USH2A HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.215901409G>C (hg19) chr1:g.215728067G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215728067G>C , CM000663.2:g.215728067G>C GRCh38
NC_000001.10:g.215901409G>C , CM000663.1:g.215901409G>C GRCh37
NC_000001.9:g.213968032G>C NCBI36
NG_009497.1:g.700330C>G
NG_009497.2:g.700382C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.12029C>G MANE Select ENSP00000305941.3:p.Thr4010Arg
ENST00000674083.1:c.12029C>G ENSP00000501296.1:p.Thr4010Arg
ENST00000307340.7:c.12029C>G ENSP00000305941.3:p.Thr4010Arg
NM_206933.2:c.12029C>G NP_996816.2:p.Thr4010Arg
NM_206933.3:c.12029C>G NP_996816.2:p.Thr4010Arg
NM_206933.4:c.12029C>G MANE Select NP_996816.3:p.Thr4010Arg
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