Canonical Allele Identifier: CA2747717675
Gene: USH2A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215675622G>T , CM000663.2:g.215675622G>T GRCh38
NC_000001.10:g.215848964G>T , CM000663.1:g.215848964G>T GRCh37
NC_000001.9:g.213915587G>T NCBI36
NG_009497.1:g.752775C>A
NG_009497.2:g.752827C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.12295-6C>A MANE Select ENSP00000305941.3:n.12295-6C>A
ENST00000674083.1:c.12295-6C>A ENSP00000501296.1:n.12295-6C>A
ENST00000307340.7:c.12295-6C>A ENSP00000305941.3:n.12295-6C>A
NM_206933.2:c.12295-6C>A NP_996816.2:n.12295-6C>A
NM_206933.3:c.12295-6C>A NP_996816.2:n.12295-6C>A
NM_206933.4:c.12295-6C>A MANE Select NP_996816.3:n.12295-6C>A
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