Canonical Allele Identifier: CA775051397
Gene: USH1G HGNC NCBI

Linked Data

dbSNP Id: rs1278266984
gnomAD v4: 17-74916370-T-C
MyVariant Identifiers: chr17:g.72912462T>C (hg19) chr17:g.74916370T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.74916370T>C , CM000679.2:g.74916370T>C GRCh38
NC_000017.10:g.72912462T>C , CM000679.1:g.72912462T>C GRCh37
NC_000017.9:g.70424057T>C NCBI36
NG_007882.1:g.11890A>G
NG_007882.2:g.11894A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000614341.5:c.*1703A>G MANE Select ENSP00000480279.1:n.*1703A>G
ENST00000614341.4:c.*1703A>G ENSP00000480279.1:n.*1703A>G
NM_001282489.2:c.*1703A>G NP_001269418.1:n.*1703A>G
NM_173477.4:c.*1703A>G NP_775748.2:n.*1703A>G
XM_011524296.1:c.*1703A>G XP_011522598.1:n.*1703A>G
XM_011524296.2:c.*1703A>G XP_011522598.1:n.*1703A>G
NM_173477.5:c.*1703A>G MANE Select NP_775748.2:n.*1703A>G
NM_001282489.3:c.*1703A>G NP_001269418.1:n.*1703A>G
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