Canonical Allele Identifier: CA310122411

Linked Data

dbSNP Id: rs1045804267
MyVariant Identifiers: chr19:g.55015976A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55015976A>G , CM000681.2:g.55015976A>G GRCh38
NC_000019.8:g.60219156A>G NCBI36
NG_031963.2:g.27289T>C , LRG_560:g.27289T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000310373.7:c.725-243T>C (GP6) ENSP00000308782.3:n.725-243T>C
ENST00000333884.2:c.671-243T>C (GP6) ENSP00000334552.2:n.671-243T>C
ENST00000417454.5:c.725-243T>C (GP6) MANE Select ENSP00000394922.1:n.725-243T>C
ENST00000465648.1:n.169-243T>C (GP6)
NM_001083899.2:c.725-243T>C , LRG_560t3:c.725-243T>C (GP6) NP_001077368.2:n.725-243T>C
NM_001256017.2:c.671-243T>C , LRG_560t2:c.671-243T>C (GP6) NP_001242946.2:n.671-243T>C
NM_016363.5:c.725-243T>C , LRG_560t1:c.725-243T>C (GP6) MANE Select NP_057447.5:n.725-243T>C
XR_001754012.2:n.312+9512A>G (GP6-AS1)
XR_001754013.2:n.305+9512A>G (GP6-AS1)