Canonical Allele Identifier: CA435769006
Gene: RHO HGNC NCBI

Linked Data

gnomAD v4: 3-129532365-C-G
MyVariant Identifiers: chr3:g.129251208C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532365C>G , CM000665.2:g.129532365C>G GRCh38
NC_000003.11:g.129251208C>G , CM000665.1:g.129251208C>G GRCh37
NC_000003.10:g.130733898C>G NCBI36
NG_009115.1:g.8727C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.645C>G MANE Select ENSP00000296271.3:p.Pro215=
ENST00000296271.3:c.645C>G ENSP00000296271.3:p.Pro215=
NM_000539.3:c.645C>G MANE Select NP_000530.1:p.Pro215=
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