Canonical Allele Identifier: CA875783951
Gene: RP2 HGNC NCBI

Linked Data

dbSNP Id: rs1251536636
gnomAD v3: X-46836949-G-T
gnomAD v4: X-46836949-G-T
MyVariant Identifiers: chrX:g.46836949G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.46836949G>T , CM000685.2:g.46836949G>T GRCh38
NC_000023.10:g.46696384G>T , CM000685.1:g.46696384G>T GRCh37
NC_000023.9:g.46581328G>T NCBI36
NG_009107.1:g.5038G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000218340.3:c.-152G>T ENSP00000218340.3:n.-152G>T
NM_006915.2:c.-152G>T NP_008846.2:n.-152G>T
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