Canonical Allele Identifier: CA1393908
Gene: USH2A HGNC NCBI

Linked Data

dbSNP Id: rs759604980

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215779935G>A , CM000663.2:g.215779935G>A GRCh38
NC_000001.10:g.215953277G>A , CM000663.1:g.215953277G>A GRCh37
NC_000001.9:g.214019900G>A NCBI36
NG_009497.1:g.648462C>T
NG_009497.2:g.648514C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.10847C>T MANE Select ENSP00000305941.3:p.Ser3616Leu
ENST00000674083.1:c.10847C>T ENSP00000501296.1:p.Ser3616Leu
ENST00000307340.7:c.10847C>T ENSP00000305941.3:p.Ser3616Leu
NM_206933.2:c.10847C>T NP_996816.2:p.Ser3616Leu
NM_206933.3:c.10847C>T NP_996816.2:p.Ser3616Leu
NM_206933.4:c.10847C>T MANE Select NP_996816.3:p.Ser3616Leu