Canonical Allele Identifier: CA344821859
Gene: USH2A HGNC NCBI

Linked Data

dbSNP Id: rs1662774023
MyVariant Identifiers: chr1:g.215987161G>C (hg19) chr1:g.215813819G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215813819G>C , CM000663.2:g.215813819G>C GRCh38
NC_000001.10:g.215987161G>C , CM000663.1:g.215987161G>C GRCh37
NC_000001.9:g.214053784G>C NCBI36
NG_009497.1:g.614578C>G
NG_009497.2:g.614630C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000307340.8:c.9656C>G MANE Select ENSP00000305941.3:p.Thr3219Ser
ENST00000674083.1:c.9656C>G ENSP00000501296.1:p.Thr3219Ser
ENST00000307340.7:c.9656C>G ENSP00000305941.3:p.Thr3219Ser
NM_206933.2:c.9656C>G NP_996816.2:p.Thr3219Ser
NM_206933.3:c.9656C>G NP_996816.2:p.Thr3219Ser
NM_206933.4:c.9656C>G MANE Select NP_996816.3:p.Thr3219Ser
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