Canonical Allele Identifier: CA450362449

Gene: PRPH2

Linked Data

• dbSNP Id: rs1761905695
• MyVariant Identifiers: chr6:g.42689527A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42721789A>G , CM000668.2:g.42721789A>G	GRCh38
NC_000006.11:g.42689527A>G , CM000668.1:g.42689527A>G	GRCh37
NC_000006.10:g.42797505A>G	NCBI36
NG_009176.1:g.5832T>C
NG_009176.2:g.5832T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230381.7:c.546T>C MANE Select	ENSP00000230381.5:p.Asn182=
ENST00000230381.6:c.546T>C	ENSP00000230381.5:p.Asn182=
NM_000322.4:c.546T>C	NP_000313.2:p.Asn182=
XR_427834.2:n.1201T>C
XR_926295.1:n.1201T>C
XR_427834.4:n.1251T>C
XR_926295.3:n.1251T>C
NM_000322.5:c.546T>C MANE Select	NP_000313.2:p.Asn182=