Canonical Allele Identifier: CA37429011

Gene: USH2A

Linked Data

• dbSNP Id: rs902502180
• MyVariant Identifiers: chr1:g.215939997T>C (hg19) ; chr1:g.215766655T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.215766655T>C , CM000663.2:g.215766655T>C	GRCh38
NC_000001.10:g.215939997T>C , CM000663.1:g.215939997T>C	GRCh37
NC_000001.9:g.214006620T>C	NCBI36
NG_009497.1:g.661742A>G
NG_009497.2:g.661794A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000307340.8:c.11047+26A>G MANE Select	ENSP00000305941.3:n.11047+26A>G
ENST00000674083.1:c.11047+26A>G	ENSP00000501296.1:n.11047+26A>G
ENST00000307340.7:c.11047+26A>G	ENSP00000305941.3:n.11047+26A>G
NM_206933.2:c.11047+26A>G	NP_996816.2:n.11047+26A>G
NM_206933.3:c.11047+26A>G	NP_996816.2:n.11047+26A>G
NM_206933.4:c.11047+26A>G MANE Select	NP_996816.3:n.11047+26A>G