Canonical Allele Identifier: CA344863450
Community Standard Title: NM_206933.4(USH2A):c.2810G>T (p.Gly937Val)
Gene: USH2A HGNC NCBI
USH2A-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.216232136C>A , CM000663.2:g.216232136C>A GRCh38
NC_000001.10:g.216405478C>A , CM000663.1:g.216405478C>A GRCh37
NC_000001.9:g.214472101C>A NCBI36
NG_009497.1:g.196261G>T
NG_009497.2:g.196313G>T

Transcript Alleles

HGVS Amino-acid Change
NM_206933.4:c.2810G>T (USH2A) MANE Select NP_996816.3:p.Gly937Val
ENST00000307340.8:c.2810G>T (USH2A) MANE Select ENSP00000305941.3:p.Gly937Val
NM_007123.5:c.2810G>T (USH2A) NP_009054.5:p.Gly937Val
NM_007123.6:c.2810G>T (USH2A) NP_009054.6:p.Gly937Val
NM_206933.2:c.2810G>T (USH2A) NP_996816.2:p.Gly937Val
NM_206933.3:c.2810G>T (USH2A) NP_996816.2:p.Gly937Val
ENST00000307340.7:c.2810G>T (USH2A) ENSP00000305941.3:p.Gly937Val
ENST00000366942.3:c.2810G>T (USH2A) ENSP00000355909.3:p.Gly937Val
ENST00000674083.1:c.2810G>T (USH2A) ENSP00000501296.1:p.Gly937Val
XR_922596.1:n.463-5699C>A (USH2A-AS1)
XR_922596.3:n.1185-5699C>A (USH2A-AS1)
XR_922597.1:n.355-5699C>A (USH2A-AS1)