Canonical Allele Identifier: CA1401209082
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs1578279516
gnomAD v4: 3-129530775-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530775A>T , CM000665.2:g.129530775A>T GRCh38
NC_000003.11:g.129249618A>T , CM000665.1:g.129249618A>T GRCh37
NC_000003.10:g.130732308A>T NCBI36
NG_009115.1:g.7137A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.362-101A>T MANE Select ENSP00000296271.3:n.362-101A>T
ENST00000296271.3:c.362-101A>T ENSP00000296271.3:n.362-101A>T
NM_000539.3:c.362-101A>T MANE Select NP_000530.1:n.362-101A>T
Search 100 bp 5'
Search 100 bp 3'