Canonical Allele Identifier: CA883669552

Linked Data

dbSNP Id: rs1568592154

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55015804A>C , CM000681.2:g.55015804A>C GRCh38
NC_000019.8:g.60218984A>C NCBI36
NG_031963.2:g.27461T>G , LRG_560:g.27461T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000310373.7:c.725-71T>G (GP6) ENSP00000308782.3:n.725-71T>G
ENST00000333884.2:c.671-71T>G (GP6) ENSP00000334552.2:n.671-71T>G
ENST00000417454.5:c.725-71T>G (GP6) MANE Select ENSP00000394922.1:n.725-71T>G
ENST00000465648.1:n.169-71T>G (GP6)
NM_001083899.2:c.725-71T>G , LRG_560t3:c.725-71T>G (GP6) NP_001077368.2:n.725-71T>G
NM_001256017.2:c.671-71T>G , LRG_560t2:c.671-71T>G (GP6) NP_001242946.2:n.671-71T>G
NM_016363.5:c.725-71T>G , LRG_560t1:c.725-71T>G (GP6) MANE Select NP_057447.5:n.725-71T>G
XR_001754012.2:n.312+9340A>C (GP6-AS1)
XR_001754013.2:n.305+9340A>C (GP6-AS1)