Canonical Allele Identifier: CA423430429
Gene: USH2A HGNC NCBI

Linked Data

dbSNP Id: rs1386988410
gnomAD v2: 1-215972451-T-G
gnomAD v4: 1-215799109-T-G
MyVariant Identifiers: chr1:g.215972451T>G (hg19) chr1:g.215799109T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215799109T>G , CM000663.2:g.215799109T>G GRCh38
NC_000001.10:g.215972451T>G , CM000663.1:g.215972451T>G GRCh37
NC_000001.9:g.214039074T>G NCBI36
NG_009497.1:g.629288A>C
NG_009497.2:g.629340A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.9756A>C MANE Select ENSP00000305941.3:p.Pro3252=
ENST00000674083.1:c.9756A>C ENSP00000501296.1:p.Pro3252=
ENST00000307340.7:c.9756A>C ENSP00000305941.3:p.Pro3252=
NM_206933.2:c.9756A>C NP_996816.2:p.Pro3252=
NM_206933.3:c.9756A>C NP_996816.2:p.Pro3252=
NM_206933.4:c.9756A>C MANE Select NP_996816.3:p.Pro3252=
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Search 100 bp 3'