Canonical Allele Identifier: CA10576378

Gene: USH2A

Linked Data

• ClinVar Variation Id: 228416
• ClinVar RCV Id: RCV000222048 ; RCV000673469 ; RCV003226253 ; RCV003445710 ; RCV003688833
• dbSNP Id: rs876657733
• gnomAD v3: 1-215877757-C-T
• gnomAD v4: 1-215877757-C-T
• MyVariant Identifiers: chr1:g.216051099C>T (hg19) ; chr1:g.215877757C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.215877757C>T , CM000663.2:g.215877757C>T	GRCh38
NC_000001.10:g.216051099C>T , CM000663.1:g.216051099C>T	GRCh37
NC_000001.9:g.214117722C>T	NCBI36
NG_009497.1:g.550640G>A
NG_009497.2:g.550692G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307340.8:c.8681+1G>A MANE Select	ENSP00000305941.3:n.8681+1G>A
ENST00000674083.1:c.8681+1G>A	ENSP00000501296.1:n.8681+1G>A
ENST00000307340.7:c.8681+1G>A	ENSP00000305941.3:n.8681+1G>A
NM_206933.2:c.8681+1G>A	NP_996816.2:n.8681+1G>A
NM_206933.3:c.8681+1G>A	NP_996816.2:n.8681+1G>A
NM_206933.4:c.8681+1G>A MANE Select	NP_996816.3:n.8681+1G>A