Canonical Allele Identifier: CA1876834682

Gene: PHF19

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120889023T>A , CM000671.2:g.120889023T>A	GRCh38
NC_000009.11:g.123651301T>A , CM000671.1:g.123651301T>A	GRCh37
NC_000009.10:g.122691122T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000616568.5:c.42+5765A>T	ENSP00000483946.1:n.42+5765A>T
ENST00000616568.4:c.42+5765A>T	ENSP00000483946.1:n.42+5765A>T
NM_001286840.1:c.42+5765A>T	NP_001273769.1:n.42+5765A>T
XM_011518511.1:c.42+5765A>T	XP_011516813.1:n.42+5765A>T
XM_011518513.1:c.-347+5765A>T	XP_011516815.1:n.-347+5765A>T
XM_011518515.1:c.42+5765A>T	XP_011516817.1:n.42+5765A>T
XM_011518516.1:c.42+5765A>T	XP_011516818.1:n.42+5765A>T
XR_929758.1:n.63+5765A>T
XR_929759.1:n.63+5765A>T
XM_011518511.2:c.42+5765A>T	XP_011516813.1:n.42+5765A>T
XM_011518515.2:c.42+5765A>T	XP_011516817.1:n.42+5765A>T
XM_011518516.2:c.42+5765A>T	XP_011516818.1:n.42+5765A>T
XM_017014612.2:c.-16+12867A>T	XP_016870101.1:n.-16+12867A>T
XM_017014613.1:c.42+5765A>T	XP_016870102.1:n.42+5765A>T
XM_024447505.1:c.-347+5765A>T	XP_024303273.1:n.-347+5765A>T
XR_929758.3:n.573+5765A>T