Canonical Allele Identifier: CA450362557
Gene: PRPH2 HGNC NCBI

Linked Data

gnomAD v4: 6-42721993-A-C
MyVariant Identifiers: chr6:g.42689731A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42721993A>C , CM000668.2:g.42721993A>C GRCh38
NC_000006.11:g.42689731A>C , CM000668.1:g.42689731A>C GRCh37
NC_000006.10:g.42797709A>C NCBI36
NG_009176.1:g.5628T>G
NG_009176.2:g.5628T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000230381.7:c.342T>G MANE Select ENSP00000230381.5:p.Leu114=
ENST00000230381.6:c.342T>G ENSP00000230381.5:p.Leu114=
NM_000322.4:c.342T>G NP_000313.2:p.Leu114=
XR_427834.2:n.997T>G
XR_926295.1:n.997T>G
XR_427834.4:n.1047T>G
XR_926295.3:n.1047T>G
NM_000322.5:c.342T>G MANE Select NP_000313.2:p.Leu114=