Canonical Allele Identifier: CA2427726121
Gene: RP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.46836950G= , CM000685.2:g.46836950G= GRCh38
NC_000023.10:g.46696385G= , CM000685.1:g.46696385G= GRCh37
NC_000023.9:g.46581329G= NCBI36
NG_009107.1:g.5039G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000218340.3:c.-151G= ENSP00000218340.3:n.-151G=
NM_006915.2:c.-151G= NP_008846.2:n.-151G=