Canonical Allele Identifier: CA364137649

Gene: PRPH2

Linked Data

• dbSNP Id: rs768473101
• MyVariant Identifiers: chr6:g.42689676C>G (hg19) ; chr6:g.42721938C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42721938C>G , CM000668.2:g.42721938C>G	GRCh38
NC_000006.11:g.42689676C>G , CM000668.1:g.42689676C>G	GRCh37
NC_000006.10:g.42797654C>G	NCBI36
NG_009176.1:g.5683G>C
NG_009176.2:g.5683G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230381.7:c.397G>C MANE Select	ENSP00000230381.5:p.Gly133Arg
ENST00000230381.6:c.397G>C	ENSP00000230381.5:p.Gly133Arg
NM_000322.4:c.397G>C	NP_000313.2:p.Gly133Arg
XR_427834.2:n.1052G>C
XR_926295.1:n.1052G>C
XR_427834.4:n.1102G>C
XR_926295.3:n.1102G>C
NM_000322.5:c.397G>C MANE Select	NP_000313.2:p.Gly133Arg