Canonical Allele Identifier: CA1220414154
Gene: USH2A HGNC NCBI

Linked Data

dbSNP Id: rs1558094144

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215779644G>A , CM000663.2:g.215779644G>A GRCh38
NC_000001.10:g.215952986G>A , CM000663.1:g.215952986G>A GRCh37
NC_000001.9:g.214019609G>A NCBI36
NG_009497.1:g.648753C>T
NG_009497.2:g.648805C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.10939+199C>T MANE Select ENSP00000305941.3:n.10939+199C>T
ENST00000674083.1:c.10939+199C>T ENSP00000501296.1:n.10939+199C>T
ENST00000307340.7:c.10939+199C>T ENSP00000305941.3:n.10939+199C>T
NM_206933.2:c.10939+199C>T NP_996816.2:n.10939+199C>T
NM_206933.3:c.10939+199C>T NP_996816.2:n.10939+199C>T
NM_206933.4:c.10939+199C>T MANE Select NP_996816.3:n.10939+199C>T