Canonical Allele Identifier: CA344834493
Gene: USH2A HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.215916519C>A (hg19) chr1:g.215743177C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215743177C>A , CM000663.2:g.215743177C>A GRCh38
NC_000001.10:g.215916519C>A , CM000663.1:g.215916519C>A GRCh37
NC_000001.9:g.213983142C>A NCBI36
NG_009497.1:g.685220G>T
NG_009497.2:g.685272G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.11548G>T MANE Select ENSP00000305941.3:p.Gly3850Ter
ENST00000674083.1:c.11548G>T ENSP00000501296.1:p.Gly3850Ter
ENST00000307340.7:c.11548G>T ENSP00000305941.3:p.Gly3850Ter
NM_206933.2:c.11548G>T NP_996816.2:p.Gly3850Ter
NM_206933.3:c.11548G>T NP_996816.2:p.Gly3850Ter
NM_206933.4:c.11548G>T MANE Select NP_996816.3:p.Gly3850Ter
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