Canonical Allele Identifier: CA423430046
Gene: USH2A HGNC NCBI

Linked Data

dbSNP Id: rs1571626719
MyVariant Identifiers: chr1:g.215901546T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215728204T>G , CM000663.2:g.215728204T>G GRCh38
NC_000001.10:g.215901546T>G , CM000663.1:g.215901546T>G GRCh37
NC_000001.9:g.213968169T>G NCBI36
NG_009497.1:g.700193A>C
NG_009497.2:g.700245A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.11892A>C MANE Select ENSP00000305941.3:p.Pro3964=
ENST00000674083.1:c.11892A>C ENSP00000501296.1:p.Pro3964=
ENST00000307340.7:c.11892A>C ENSP00000305941.3:p.Pro3964=
NM_206933.2:c.11892A>C NP_996816.2:p.Pro3964=
NM_206933.3:c.11892A>C NP_996816.2:p.Pro3964=
NM_206933.4:c.11892A>C MANE Select NP_996816.3:p.Pro3964=