Canonical Allele Identifier: CA1393155

Gene: USH2A

Linked Data

• ClinVar Variation Id: 289390
• ClinVar RCV Id: RCV000395763 ; RCV001272938
• dbSNP Id: rs370364142
• ExAC: 1:215844374 G / A
• gnomAD v2: 1-215844374-G-A
• gnomAD v3: 1-215671032-G-A
• gnomAD v4: 1-215671032-G-A
• COSMIC: COSM463930
• MyVariant Identifiers: chr1:g.215844374G>A (hg19) ; chr1:g.215671032G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.215671032G>A , CM000663.2:g.215671032G>A	GRCh38
NC_000001.10:g.215844374G>A , CM000663.1:g.215844374G>A	GRCh37
NC_000001.9:g.213910997G>A	NCBI36
NG_009497.1:g.757365C>T
NG_009497.2:g.757417C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307340.8:c.14073C>T MANE Select	ENSP00000305941.3:p.Asn4691=
ENST00000674083.1:c.14073C>T	ENSP00000501296.1:p.Asn4691=
ENST00000307340.7:c.14073C>T	ENSP00000305941.3:p.Asn4691=
NM_206933.2:c.14073C>T	NP_996816.2:p.Asn4691=
NM_206933.3:c.14073C>T	NP_996816.2:p.Asn4691=
NM_206933.4:c.14073C>T MANE Select	NP_996816.3:p.Asn4691=