Canonical Allele Identifier: CA1012184990

Gene: USH2A

Linked Data

• gnomAD v3: 1-215640830-C-A
• gnomAD v4: 1-215640830-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.215640830C>A , CM000663.2:g.215640830C>A	GRCh38
NC_000001.10:g.215814172C>A , CM000663.1:g.215814172C>A	GRCh37
NC_000001.9:g.213880795C>A	NCBI36
NG_009497.1:g.787567G>T
NG_009497.2:g.787619G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307340.8:c.14792-96G>T MANE Select	ENSP00000305941.3:n.14792-96G>T
ENST00000674083.1:c.14792-96G>T	ENSP00000501296.1:n.14792-96G>T
ENST00000307340.7:c.14792-96G>T	ENSP00000305941.3:n.14792-96G>T
NM_206933.2:c.14792-96G>T	NP_996816.2:n.14792-96G>T
NM_206933.3:c.14792-96G>T	NP_996816.2:n.14792-96G>T
NM_206933.4:c.14792-96G>T MANE Select	NP_996816.3:n.14792-96G>T