Canonical Allele Identifier: CA657970909
Gene: RP2 HGNC NCBI

Linked Data

dbSNP Id: rs1211364998
gnomAD v3: X-46837006-G-A
gnomAD v4: X-46837006-G-A
COSMIC: COSN24391906
MyVariant Identifiers: chrX:g.46837006G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.46837006G>A , CM000685.2:g.46837006G>A GRCh38
NC_000023.10:g.46696441G>A , CM000685.1:g.46696441G>A GRCh37
NC_000023.9:g.46581385G>A NCBI36
NG_009107.1:g.5095G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000218340.3:c.-95G>A ENSP00000218340.3:n.-95G>A
NM_006915.2:c.-95G>A NP_008846.2:n.-95G>A
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