Canonical Allele Identifier: CA407479229
Gene: GP6 HGNC NCBI
GP6-AS1 HGNC NCBI

Linked Data

gnomAD v4: 19-55015716-T-C
MyVariant Identifiers: chr19:g.55015716T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55015716T>C , CM000681.2:g.55015716T>C GRCh38
NC_000019.8:g.60218896T>C NCBI36
NG_031963.2:g.27549A>G , LRG_560:g.27549A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000310373.7:c.742A>G (GP6) ENSP00000308782.3:p.Thr248Ala
ENST00000333884.2:c.688A>G (GP6) ENSP00000334552.2:p.Thr230Ala
ENST00000417454.5:c.742A>G (GP6) MANE Select ENSP00000394922.1:p.Thr248Ala
ENST00000465648.1:n.186A>G (GP6)
NM_001083899.2:c.742A>G , LRG_560t3:c.742A>G (GP6) NP_001077368.2:p.Thr248Ala
NM_001256017.2:c.688A>G , LRG_560t2:c.688A>G (GP6) NP_001242946.2:p.Thr230Ala
NM_016363.5:c.742A>G , LRG_560t1:c.742A>G (GP6) MANE Select NP_057447.5:p.Thr248Ala
XR_001754012.2:n.312+9252T>C (GP6-AS1)
XR_001754013.2:n.305+9252T>C (GP6-AS1)
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