Canonical Allele Identifier: CA1393945

Gene: USH2A

Linked Data

• dbSNP Id: rs774504874
• ExAC: 1:215955350 C / A
• gnomAD v2: 1-215955350-C-A
• gnomAD v4: 1-215782008-C-A
• MyVariant Identifiers: chr1:g.215955350C>A (hg19) ; chr1:g.215782008C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.215782008C>A , CM000663.2:g.215782008C>A	GRCh38
NC_000001.10:g.215955350C>A , CM000663.1:g.215955350C>A	GRCh37
NC_000001.9:g.214021973C>A	NCBI36
NG_009497.1:g.646389G>T
NG_009497.2:g.646441G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000307340.8:c.10740+34G>T MANE Select	ENSP00000305941.3:n.10740+34G>T
ENST00000674083.1:c.10740+34G>T	ENSP00000501296.1:n.10740+34G>T
ENST00000307340.7:c.10740+34G>T	ENSP00000305941.3:n.10740+34G>T
NM_206933.2:c.10740+34G>T	NP_996816.2:n.10740+34G>T
NM_206933.3:c.10740+34G>T	NP_996816.2:n.10740+34G>T
NM_206933.4:c.10740+34G>T MANE Select	NP_996816.3:n.10740+34G>T