Canonical Allele Identifier: CA2747716398
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215640771C>A , CM000663.2:g.215640771C>A GRCh38
NC_000001.10:g.215814113C>A , CM000663.1:g.215814113C>A GRCh37
NC_000001.9:g.213880736C>A NCBI36
NG_009497.1:g.787626G>T
NG_009497.2:g.787678G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.14792-37G>T MANE Select ENSP00000305941.3:n.14792-37G>T
ENST00000674083.1:c.14792-37G>T ENSP00000501296.1:n.14792-37G>T
ENST00000307340.7:c.14792-37G>T ENSP00000305941.3:n.14792-37G>T
NM_206933.2:c.14792-37G>T NP_996816.2:n.14792-37G>T
NM_206933.3:c.14792-37G>T NP_996816.2:n.14792-37G>T
NM_206933.4:c.14792-37G>T MANE Select NP_996816.3:n.14792-37G>T