Canonical Allele Identifier: CA2667617014
Gene: RHO HGNC NCBI

Linked Data

gnomAD v4: 3-129532422-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532422G>T , CM000665.2:g.129532422G>T GRCh38
NC_000003.11:g.129251265G>T , CM000665.1:g.129251265G>T GRCh37
NC_000003.10:g.130733955G>T NCBI36
NG_009115.1:g.8784G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.696+6G>T MANE Select ENSP00000296271.3:n.696+6G>T
ENST00000296271.3:c.696+6G>T ENSP00000296271.3:n.696+6G>T
NM_000539.3:c.696+6G>T MANE Select NP_000530.1:n.696+6G>T
Search 100 bp 5'
Search 100 bp 3'