Canonical Allele Identifier: CA3808630
Gene: PRPH2 HGNC NCBI

Linked Data

dbSNP Id: rs753507738
gnomAD v2: 6-42689710-C-G
gnomAD v4: 6-42721972-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42721972C>G , CM000668.2:g.42721972C>G GRCh38
NC_000006.11:g.42689710C>G , CM000668.1:g.42689710C>G GRCh37
NC_000006.10:g.42797688C>G NCBI36
NG_009176.1:g.5649G>C
NG_009176.2:g.5649G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000230381.7:c.363G>C MANE Select ENSP00000230381.5:p.Leu121=
ENST00000230381.6:c.363G>C ENSP00000230381.5:p.Leu121=
NM_000322.4:c.363G>C NP_000313.2:p.Leu121=
XR_427834.2:n.1018G>C
XR_926295.1:n.1018G>C
XR_427834.4:n.1068G>C
XR_926295.3:n.1068G>C
NM_000322.5:c.363G>C MANE Select NP_000313.2:p.Leu121=