Canonical Allele Identifier: CA37444219
Gene: USH2A HGNC NCBI

Linked Data

dbSNP Id: rs977854773
MyVariant Identifiers: chr1:g.216019091G>C (hg19) chr1:g.215845749G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215845749G>C , CM000663.2:g.215845749G>C GRCh38
NC_000001.10:g.216019091G>C , CM000663.1:g.216019091G>C GRCh37
NC_000001.9:g.214085714G>C NCBI36
NG_009497.1:g.582648C>G
NG_009497.2:g.582700C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000307340.8:c.9055+75C>G MANE Select ENSP00000305941.3:n.9055+75C>G
ENST00000674083.1:c.9055+75C>G ENSP00000501296.1:n.9055+75C>G
ENST00000307340.7:c.9055+75C>G ENSP00000305941.3:n.9055+75C>G
NM_206933.2:c.9055+75C>G NP_996816.2:n.9055+75C>G
NM_206933.3:c.9055+75C>G NP_996816.2:n.9055+75C>G
NM_206933.4:c.9055+75C>G MANE Select NP_996816.3:n.9055+75C>G
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