Canonical Allele Identifier: CA344849694

Gene: USH2A

Linked Data

• MyVariant Identifiers: chr1:g.215972407C>T (hg19) ; chr1:g.215799065C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.215799065C>T , CM000663.2:g.215799065C>T	GRCh38
NC_000001.10:g.215972407C>T , CM000663.1:g.215972407C>T	GRCh37
NC_000001.9:g.214039030C>T	NCBI36
NG_009497.1:g.629332G>A
NG_009497.2:g.629384G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307340.8:c.9800G>A MANE Select	ENSP00000305941.3:p.Cys3267Tyr
ENST00000674083.1:c.9800G>A	ENSP00000501296.1:p.Cys3267Tyr
ENST00000307340.7:c.9800G>A	ENSP00000305941.3:p.Cys3267Tyr
NM_206933.2:c.9800G>A	NP_996816.2:p.Cys3267Tyr
NM_206933.3:c.9800G>A	NP_996816.2:p.Cys3267Tyr
NM_206933.4:c.9800G>A MANE Select	NP_996816.3:p.Cys3267Tyr