Canonical Allele Identifier: CA997224692

Linked Data

dbSNP Id: rs1568591375

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55015615C>G , CM000681.2:g.55015615C>G GRCh38
NC_000019.8:g.60218795C>G NCBI36
NG_031963.2:g.27650G>C , LRG_560:g.27650G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000310373.7:c.779+64G>C (GP6) ENSP00000308782.3:n.779+64G>C
ENST00000333884.2:c.721+68G>C (GP6) ENSP00000334552.2:n.721+68G>C
ENST00000417454.5:c.775+68G>C (GP6) MANE Select ENSP00000394922.1:n.775+68G>C
ENST00000465648.1:n.219+68G>C (GP6)
NM_001083899.2:c.779+64G>C , LRG_560t3:c.779+64G>C (GP6) NP_001077368.2:n.779+64G>C
NM_001256017.2:c.721+68G>C , LRG_560t2:c.721+68G>C (GP6) NP_001242946.2:n.721+68G>C
NM_016363.5:c.775+68G>C , LRG_560t1:c.775+68G>C (GP6) MANE Select NP_057447.5:n.775+68G>C
XR_001754012.2:n.312+9151C>G (GP6-AS1)
XR_001754013.2:n.305+9151C>G (GP6-AS1)