Canonical Allele Identifier: CA354469856
Gene: RHO HGNC NCBI

Linked Data

gnomAD v4: 3-129532341-G-A
MyVariant Identifiers: chr3:g.129251184G>A (hg19) chr3:g.129532341G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532341G>A , CM000665.2:g.129532341G>A GRCh38
NC_000003.11:g.129251184G>A , CM000665.1:g.129251184G>A GRCh37
NC_000003.10:g.130733874G>A NCBI36
NG_009115.1:g.8703G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.621G>A MANE Select ENSP00000296271.3:p.Met207Ile
ENST00000296271.3:c.621G>A ENSP00000296271.3:p.Met207Ile
NM_000539.3:c.621G>A MANE Select NP_000530.1:p.Met207Ile
Search 100 bp 5'
Search 100 bp 3'