Canonical Allele Identifier: CA423428441
Gene: USH2A HGNC NCBI

Linked Data

dbSNP Id: rs2797235
MyVariant Identifiers: chr1:g.215848641T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215675299T>A , CM000663.2:g.215675299T>A GRCh38
NC_000001.10:g.215848641T>A , CM000663.1:g.215848641T>A GRCh37
NC_000001.9:g.213915264T>A NCBI36
NG_009497.2:g.753150A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.12612A>T MANE Select ENSP00000305941.3:p.Thr4204=
ENST00000674083.1:c.12612A>T ENSP00000501296.1:p.Thr4204=
ENST00000307340.7:c.12612A>T ENSP00000305941.3:p.Thr4204=
NM_206933.4:c.12612A>T MANE Select NP_996816.3:p.Thr4204=