Canonical Allele Identifier: CA2427731432
Gene: RP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.46853769C= , CM000685.2:g.46853769C= GRCh38
NC_000023.10:g.46713204C= , CM000685.1:g.46713204C= GRCh37
NC_000023.9:g.46598148C= NCBI36
NG_009107.1:g.21858C=

Transcript Alleles

HGVS Amino-acid change
ENST00000218340.4:c.396C= MANE Select ENSP00000218340.3:p.Ala132=
ENST00000218340.3:c.396C= ENSP00000218340.3:p.Ala132=
NM_006915.2:c.396C= NP_008846.2:p.Ala132=
NM_006915.3:c.396C= MANE Select NP_008846.2:p.Ala132=