Canonical Allele Identifier: CA344829791
Gene: USH2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215728360C>G , CM000663.2:g.215728360C>G GRCh38
NC_000001.10:g.215901702C>G , CM000663.1:g.215901702C>G GRCh37
NC_000001.9:g.213968325C>G NCBI36
NG_009497.1:g.700037G>C
NG_009497.2:g.700089G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.11736G>C MANE Select ENSP00000305941.3:p.Glu3912Asp
ENST00000674083.1:c.11736G>C ENSP00000501296.1:p.Glu3912Asp
ENST00000307340.7:c.11736G>C ENSP00000305941.3:p.Glu3912Asp
NM_206933.2:c.11736G>C NP_996816.2:p.Glu3912Asp
NM_206933.3:c.11736G>C NP_996816.2:p.Glu3912Asp
NM_206933.4:c.11736G>C MANE Select NP_996816.3:p.Glu3912Asp