Canonical Allele Identifier: CA344824022
Gene: USH2A HGNC NCBI

Linked Data

dbSNP Id: rs1662876606
gnomAD v4: 1-215817012-A-C
MyVariant Identifiers: chr1:g.215990354A>C (hg19) chr1:g.215817012A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215817012A>C , CM000663.2:g.215817012A>C GRCh38
NC_000001.10:g.215990354A>C , CM000663.1:g.215990354A>C GRCh37
NC_000001.9:g.214056977A>C NCBI36
NG_009497.1:g.611385T>G
NG_009497.2:g.611437T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.9555T>G MANE Select ENSP00000305941.3:p.Tyr3185Ter
ENST00000674083.1:c.9555T>G ENSP00000501296.1:p.Tyr3185Ter
ENST00000307340.7:c.9555T>G ENSP00000305941.3:p.Tyr3185Ter
NM_206933.2:c.9555T>G NP_996816.2:p.Tyr3185Ter
NM_206933.3:c.9555T>G NP_996816.2:p.Tyr3185Ter
NM_206933.4:c.9555T>G MANE Select NP_996816.3:p.Tyr3185Ter
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