Canonical Allele Identifier: CA423306869

Gene: USH2A

Linked Data

• MyVariant Identifiers: chr1:g.215813973C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.215640631C>A , CM000663.2:g.215640631C>A	GRCh38
NC_000001.10:g.215813973C>A , CM000663.1:g.215813973C>A	GRCh37
NC_000001.9:g.213880596C>A	NCBI36
NG_009497.1:g.787766G>T
NG_009497.2:g.787818G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307340.8:c.14895G>T MANE Select	ENSP00000305941.3:p.Val4965=
ENST00000674083.1:c.14895G>T	ENSP00000501296.1:p.Val4965=
ENST00000307340.7:c.14895G>T	ENSP00000305941.3:p.Val4965=
NM_206933.2:c.14895G>T	NP_996816.2:p.Val4965=
NM_206933.3:c.14895G>T	NP_996816.2:p.Val4965=
NM_206933.4:c.14895G>T MANE Select	NP_996816.3:p.Val4965=