Canonical Allele Identifier: CA997224798

Linked Data

dbSNP Id: rs1449336138

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55015967A>C , CM000681.2:g.55015967A>C GRCh38
NC_000019.8:g.60219147A>C NCBI36
NG_031963.2:g.27298T>G , LRG_560:g.27298T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000310373.7:c.725-234T>G (GP6) ENSP00000308782.3:n.725-234T>G
ENST00000333884.2:c.671-234T>G (GP6) ENSP00000334552.2:n.671-234T>G
ENST00000417454.5:c.725-234T>G (GP6) MANE Select ENSP00000394922.1:n.725-234T>G
ENST00000465648.1:n.169-234T>G (GP6)
NM_001083899.2:c.725-234T>G , LRG_560t3:c.725-234T>G (GP6) NP_001077368.2:n.725-234T>G
NM_001256017.2:c.671-234T>G , LRG_560t2:c.671-234T>G (GP6) NP_001242946.2:n.671-234T>G
NM_016363.5:c.725-234T>G , LRG_560t1:c.725-234T>G (GP6) MANE Select NP_057447.5:n.725-234T>G
XR_001754012.2:n.312+9503A>C (GP6-AS1)
XR_001754013.2:n.305+9503A>C (GP6-AS1)