Canonical Allele Identifier: CA344826991
Gene: USH2A HGNC NCBI

Linked Data

gnomAD v4: 1-215728079-G-A
MyVariant Identifiers: chr1:g.215901421G>A (hg19) chr1:g.215728079G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215728079G>A , CM000663.2:g.215728079G>A GRCh38
NC_000001.10:g.215901421G>A , CM000663.1:g.215901421G>A GRCh37
NC_000001.9:g.213968044G>A NCBI36
NG_009497.1:g.700318C>T
NG_009497.2:g.700370C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.12017C>T MANE Select ENSP00000305941.3:p.Pro4006Leu
ENST00000674083.1:c.12017C>T ENSP00000501296.1:p.Pro4006Leu
ENST00000307340.7:c.12017C>T ENSP00000305941.3:p.Pro4006Leu
NM_206933.2:c.12017C>T NP_996816.2:p.Pro4006Leu
NM_206933.3:c.12017C>T NP_996816.2:p.Pro4006Leu
NM_206933.4:c.12017C>T MANE Select NP_996816.3:p.Pro4006Leu
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