Canonical Allele Identifier: CA2427726132
Gene: RP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.46836962A= , CM000685.2:g.46836962A= GRCh38
NC_000023.10:g.46696397A= , CM000685.1:g.46696397A= GRCh37
NC_000023.9:g.46581341A= NCBI36
NG_009107.1:g.5051A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000218340.3:c.-139A= ENSP00000218340.3:n.-139A=
NM_006915.2:c.-139A= NP_008846.2:n.-139A=