Canonical Allele Identifier: CA82647278
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs879100706
gnomAD v2: 3-129248170-C-T
gnomAD v3: 3-129529327-C-T
gnomAD v4: 3-129529327-C-T
MyVariant Identifiers: chr3:g.129248170C>T (hg19) chr3:g.129529327C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129529327C>T , CM000665.2:g.129529327C>T GRCh38
NC_000003.11:g.129248170C>T , CM000665.1:g.129248170C>T GRCh37
NC_000003.10:g.130730860C>T NCBI36
NG_009115.1:g.5689C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.361+233C>T MANE Select ENSP00000296271.3:n.361+233C>T
ENST00000296271.3:c.361+233C>T ENSP00000296271.3:n.361+233C>T
NM_000539.3:c.361+233C>T MANE Select NP_000530.1:n.361+233C>T
Search 100 bp 5'
Search 100 bp 3'