Canonical Allele Identifier: CA1401209089
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs2084774041
gnomAD v4: 3-129530780-T-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530780T>C , CM000665.2:g.129530780T>C GRCh38
NC_000003.11:g.129249623T>C , CM000665.1:g.129249623T>C GRCh37
NC_000003.10:g.130732313T>C NCBI36
NG_009115.1:g.7142T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.362-96T>C MANE Select ENSP00000296271.3:n.362-96T>C
ENST00000296271.3:c.362-96T>C ENSP00000296271.3:n.362-96T>C
NM_000539.3:c.362-96T>C MANE Select NP_000530.1:n.362-96T>C
Search 100 bp 5'
Search 100 bp 3'