Canonical Allele Identifier: CA875783945
Gene: RP2 HGNC NCBI

Linked Data

dbSNP Id: rs1246632967
gnomAD v3: X-46836922-G-T
gnomAD v4: X-46836922-G-T
MyVariant Identifiers: chrX:g.46836922G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.46836922G>T , CM000685.2:g.46836922G>T GRCh38
NC_000023.10:g.46696357G>T , CM000685.1:g.46696357G>T GRCh37
NC_000023.9:g.46581301G>T NCBI36
NG_009107.1:g.5011G>T

Transcript Alleles

HGVS Amino-acid Change
NM_006915.2:c.-179G>T NP_008846.2:n.-179G>T
Search 100 bp 5'
Search 100 bp 3'