Canonical Allele Identifier: CA344816452
Gene: USH2A HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.215853631T>C (hg19) chr1:g.215680289T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215680289T>C , CM000663.2:g.215680289T>C GRCh38
NC_000001.10:g.215853631T>C , CM000663.1:g.215853631T>C GRCh37
NC_000001.9:g.213920254T>C NCBI36
NG_009497.1:g.748108A>G
NG_009497.2:g.748160A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000307340.8:c.12154A>G MANE Select ENSP00000305941.3:p.Ile4052Val
ENST00000674083.1:c.12154A>G ENSP00000501296.1:p.Ile4052Val
ENST00000307340.7:c.12154A>G ENSP00000305941.3:p.Ile4052Val
NM_206933.2:c.12154A>G NP_996816.2:p.Ile4052Val
NM_206933.3:c.12154A>G NP_996816.2:p.Ile4052Val
NM_206933.4:c.12154A>G MANE Select NP_996816.3:p.Ile4052Val
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