Canonical Allele Identifier: CA2747717494
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215671352A>C , CM000663.2:g.215671352A>C GRCh38
NC_000001.10:g.215844694A>C , CM000663.1:g.215844694A>C GRCh37
NC_000001.9:g.213911317A>C NCBI36
NG_009497.1:g.757045T>G
NG_009497.2:g.757097T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.13812-59T>G MANE Select ENSP00000305941.3:n.13812-59T>G
ENST00000674083.1:c.13812-59T>G ENSP00000501296.1:n.13812-59T>G
ENST00000307340.7:c.13812-59T>G ENSP00000305941.3:n.13812-59T>G
NM_206933.2:c.13812-59T>G NP_996816.2:n.13812-59T>G
NM_206933.3:c.13812-59T>G NP_996816.2:n.13812-59T>G
NM_206933.4:c.13812-59T>G MANE Select NP_996816.3:n.13812-59T>G