Canonical Allele Identifier: CA1053434645
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs2084760607
gnomAD v3: 3-129529291-A-C
gnomAD v4: 3-129529291-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129529291A>C , CM000665.2:g.129529291A>C GRCh38
NC_000003.11:g.129248134A>C , CM000665.1:g.129248134A>C GRCh37
NC_000003.10:g.130730824A>C NCBI36
NG_009115.1:g.5653A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.361+197A>C MANE Select ENSP00000296271.3:n.361+197A>C
ENST00000296271.3:c.361+197A>C ENSP00000296271.3:n.361+197A>C
NM_000539.3:c.361+197A>C MANE Select NP_000530.1:n.361+197A>C
Search 100 bp 5'
Search 100 bp 3'