Canonical Allele Identifier: CA344826698
Gene: USH2A HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.215901372C>G (hg19) chr1:g.215728030C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215728030C>G , CM000663.2:g.215728030C>G GRCh38
NC_000001.10:g.215901372C>G , CM000663.1:g.215901372C>G GRCh37
NC_000001.9:g.213967995C>G NCBI36
NG_009497.1:g.700367G>C
NG_009497.2:g.700419G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.12066G>C MANE Select ENSP00000305941.3:p.Lys4022Asn
ENST00000674083.1:c.12066G>C ENSP00000501296.1:p.Lys4022Asn
ENST00000307340.7:c.12066G>C ENSP00000305941.3:p.Lys4022Asn
NM_206933.2:c.12066G>C NP_996816.2:p.Lys4022Asn
NM_206933.3:c.12066G>C NP_996816.2:p.Lys4022Asn
NM_206933.4:c.12066G>C MANE Select NP_996816.3:p.Lys4022Asn
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