Canonical Allele Identifier: CA290332058

Gene: PCGF2

Linked Data

• ClinVar Variation Id: 1902007
• ClinVar RCV Id: RCV002579962
• dbSNP Id: rs771052318
• gnomAD v2: 17-36892327-C-T
• gnomAD v3: 17-38736074-C-T
• gnomAD v4: 17-38736074-C-T
• MyVariant Identifiers: chr17:g.36892327C>T (hg19) ; chr17:g.38736074C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.38736074C>T , CM000679.2:g.38736074C>T	GRCh38
NC_000017.10:g.36892327C>T , CM000679.1:g.36892327C>T	GRCh37
NC_000017.9:g.34145853C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620225.5:c.657+16G>A MANE Select	ENSP00000482815.1:n.657+16G>A
ENST00000611883.4:c.657+16G>A	ENSP00000478970.1:n.657+16G>A
ENST00000616129.4:c.661+16G>A	ENSP00000484201.1:n.661+16G>A
ENST00000616199.4:c.657+16G>A	ENSP00000482063.1:n.657+16G>A
ENST00000618506.1:c.499+16G>A	ENSP00000484721.1:n.499+16G>A
ENST00000618941.4:c.661+16G>A	ENSP00000481656.1:n.661+16G>A
ENST00000620225.4:c.657+16G>A	ENSP00000482815.1:n.657+16G>A
NM_007144.2:c.657+16G>A	NP_009075.1:n.657+16G>A
XM_005257640.1:c.657+16G>A	XP_005257697.1:n.657+16G>A
XM_005257641.3:c.657+16G>A	XP_005257698.1:n.657+16G>A
XM_005257642.2:c.657+16G>A	XP_005257699.1:n.657+16G>A
XM_005257640.2:c.657+16G>A	XP_005257697.1:n.657+16G>A
XM_005257641.5:c.657+16G>A	XP_005257698.1:n.657+16G>A
XM_005257642.3:c.657+16G>A	XP_005257699.1:n.657+16G>A
XM_017025016.1:c.657+16G>A	XP_016880505.1:n.657+16G>A
NM_007144.3:c.657+16G>A MANE Select	NP_009075.1:n.657+16G>A
NM_001369614.1:c.657+16G>A	NP_001356543.1:n.657+16G>A
NM_001369615.1:c.657+16G>A	NP_001356544.1:n.657+16G>A