Canonical Allele Identifier: CA1220417047

Gene: USH2A

Linked Data

• dbSNP Id: rs1661670932

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.215782458C>A , CM000663.2:g.215782458C>A	GRCh38
NC_000001.10:g.215955800C>A , CM000663.1:g.215955800C>A	GRCh37
NC_000001.9:g.214022423C>A	NCBI36
NG_009497.1:g.645939G>T
NG_009497.2:g.645991G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307340.8:c.10586-262G>T MANE Select	ENSP00000305941.3:n.10586-262G>T
ENST00000674083.1:c.10586-262G>T	ENSP00000501296.1:n.10586-262G>T
ENST00000307340.7:c.10586-262G>T	ENSP00000305941.3:n.10586-262G>T
NM_206933.2:c.10586-262G>T	NP_996816.2:n.10586-262G>T
NM_206933.3:c.10586-262G>T	NP_996816.2:n.10586-262G>T
NM_206933.4:c.10586-262G>T MANE Select	NP_996816.3:n.10586-262G>T