Canonical Allele Identifier: CA344824168

Gene: USH2A

Linked Data

• MyVariant Identifiers: chr1:g.215990368C>T (hg19) ; chr1:g.215817026C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.215817026C>T , CM000663.2:g.215817026C>T	GRCh38
NC_000001.10:g.215990368C>T , CM000663.1:g.215990368C>T	GRCh37
NC_000001.9:g.214056991C>T	NCBI36
NG_009497.1:g.611371G>A
NG_009497.2:g.611423G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307340.8:c.9541G>A MANE Select	ENSP00000305941.3:p.Gly3181Arg
ENST00000674083.1:c.9541G>A	ENSP00000501296.1:p.Gly3181Arg
ENST00000307340.7:c.9541G>A	ENSP00000305941.3:p.Gly3181Arg
NM_206933.2:c.9541G>A	NP_996816.2:p.Gly3181Arg
NM_206933.3:c.9541G>A	NP_996816.2:p.Gly3181Arg
NM_206933.4:c.9541G>A MANE Select	NP_996816.3:p.Gly3181Arg