Canonical Allele Identifier: CA364135342

Gene: PRPH2

Linked Data

• MyVariant Identifiers: chr6:g.42672249T>A (hg19) ; chr6:g.42704511T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42704511T>A , CM000668.2:g.42704511T>A	GRCh38
NC_000006.11:g.42672249T>A , CM000668.1:g.42672249T>A	GRCh37
NC_000006.10:g.42780227T>A	NCBI36
NG_009176.1:g.23110A>T
NG_009176.2:g.23110A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000230381.7:c.682A>T MANE Select	ENSP00000230381.5:p.Thr228Ser
ENST00000230381.6:c.682A>T	ENSP00000230381.5:p.Thr228Ser
NM_000322.4:c.682A>T	NP_000313.2:p.Thr228Ser
XR_427834.2:n.1337A>T
XR_427834.4:n.1387A>T
XR_926295.3:n.1569A>T
NM_000322.5:c.682A>T MANE Select	NP_000313.2:p.Thr228Ser