Canonical Allele Identifier: CA344851145
Gene: USH2A HGNC NCBI

Linked Data

dbSNP Id: rs1657994575

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215675547G>T , CM000663.2:g.215675547G>T GRCh38
NC_000001.10:g.215848889G>T , CM000663.1:g.215848889G>T GRCh37
NC_000001.9:g.213915512G>T NCBI36
NG_009497.1:g.752850C>A
NG_009497.2:g.752902C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.12364C>A MANE Select ENSP00000305941.3:p.Leu4122Met
ENST00000674083.1:c.12364C>A ENSP00000501296.1:p.Leu4122Met
ENST00000307340.7:c.12364C>A ENSP00000305941.3:p.Leu4122Met
NM_206933.2:c.12364C>A NP_996816.2:p.Leu4122Met
NM_206933.3:c.12364C>A NP_996816.2:p.Leu4122Met
NM_206933.4:c.12364C>A MANE Select NP_996816.3:p.Leu4122Met