Canonical Allele Identifier: CA1053435870
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs2084773903
gnomAD v3: 3-129530765-T-TCCCTCTCCCACTCCTGGTTGCCTTCCTAGCTA
gnomAD v4: 3-129530765-T-TCCCTCTCCCACTCCTGGTTGCCTTCCTAGCTA
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530775_129530806dup , CM000665.2:g.129530775_129530806dup GRCh38
NC_000003.11:g.129249618_129249649dup , CM000665.1:g.129249618_129249649dup GRCh37
NC_000003.10:g.130732308_130732339dup NCBI36
NG_009115.1:g.7137_7168dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-101_362-70dup MANE Select ENSP00000296271.3:n.362-101_362-70dup
ENST00000296271.3:c.362-101_362-70dup ENSP00000296271.3:n.362-101_362-70dup
NM_000539.3:c.362-101_362-70dup MANE Select NP_000530.1:n.362-101_362-70dup
Search 100 bp 5'
Search 100 bp 3'