Canonical Allele Identifier: CA2427726161
Gene: RP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.46837002G= , CM000685.2:g.46837002G= GRCh38
NC_000023.10:g.46696437G= , CM000685.1:g.46696437G= GRCh37
NC_000023.9:g.46581381G= NCBI36
NG_009107.1:g.5091G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000218340.3:c.-99G= ENSP00000218340.3:n.-99G=
NM_006915.2:c.-99G= NP_008846.2:n.-99G=