Canonical Allele Identifier: CA883669445

Linked Data

dbSNP Id: rs1332102886
MyVariant Identifiers: chr19:g.55015723C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55015723C>T , CM000681.2:g.55015723C>T GRCh38
NC_000019.8:g.60218903C>T NCBI36
NG_031963.2:g.27542G>A , LRG_560:g.27542G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000310373.7:c.735G>A (GP6) ENSP00000308782.3:p.Arg245=
ENST00000333884.2:c.681G>A (GP6) ENSP00000334552.2:p.Arg227=
ENST00000417454.5:c.735G>A (GP6) MANE Select ENSP00000394922.1:p.Arg245=
ENST00000465648.1:n.179G>A (GP6)
NM_001083899.2:c.735G>A , LRG_560t3:c.735G>A (GP6) NP_001077368.2:p.Arg245=
NM_001256017.2:c.681G>A , LRG_560t2:c.681G>A (GP6) NP_001242946.2:p.Arg227=
NM_016363.5:c.735G>A , LRG_560t1:c.735G>A (GP6) MANE Select NP_057447.5:p.Arg245=
XR_001754012.2:n.312+9259C>T (GP6-AS1)
XR_001754013.2:n.305+9259C>T (GP6-AS1)