Canonical Allele Identifier: CA1012185405
Gene: USH2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215640883T>A , CM000663.2:g.215640883T>A GRCh38
NC_000001.10:g.215814225T>A , CM000663.1:g.215814225T>A GRCh37
NC_000001.9:g.213880848T>A NCBI36
NG_009497.1:g.787514A>T
NG_009497.2:g.787566A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.14792-149A>T MANE Select ENSP00000305941.3:n.14792-149A>T
ENST00000674083.1:c.14792-149A>T ENSP00000501296.1:n.14792-149A>T
ENST00000307340.7:c.14792-149A>T ENSP00000305941.3:n.14792-149A>T
NM_206933.2:c.14792-149A>T NP_996816.2:n.14792-149A>T
NM_206933.3:c.14792-149A>T NP_996816.2:n.14792-149A>T
NM_206933.4:c.14792-149A>T MANE Select NP_996816.3:n.14792-149A>T