Canonical Allele Identifier: CA344850136
Gene: USH2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215799110G>T , CM000663.2:g.215799110G>T GRCh38
NC_000001.10:g.215972452G>T , CM000663.1:g.215972452G>T GRCh37
NC_000001.9:g.214039075G>T NCBI36
NG_009497.1:g.629287C>A
NG_009497.2:g.629339C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.9755C>A MANE Select ENSP00000305941.3:p.Pro3252Gln
ENST00000674083.1:c.9755C>A ENSP00000501296.1:p.Pro3252Gln
ENST00000307340.7:c.9755C>A ENSP00000305941.3:p.Pro3252Gln
NM_206933.2:c.9755C>A NP_996816.2:p.Pro3252Gln
NM_206933.3:c.9755C>A NP_996816.2:p.Pro3252Gln
NM_206933.4:c.9755C>A MANE Select NP_996816.3:p.Pro3252Gln