Canonical Allele Identifier: CA1876835413

Gene: PHF19

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120890620T= , CM000671.2:g.120890620T=	GRCh38
NC_000009.11:g.123652898T= , CM000671.1:g.123652898T=	GRCh37
NC_000009.10:g.122692719T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000616568.5:c.42+4168A=	ENSP00000483946.1:n.42+4168A=
ENST00000616568.4:c.42+4168A=	ENSP00000483946.1:n.42+4168A=
NM_001286840.1:c.42+4168A=	NP_001273769.1:n.42+4168A=
XM_011518511.1:c.42+4168A=	XP_011516813.1:n.42+4168A=
XM_011518513.1:c.-347+4168A=	XP_011516815.1:n.-347+4168A=
XM_011518515.1:c.42+4168A=	XP_011516817.1:n.42+4168A=
XM_011518516.1:c.42+4168A=	XP_011516818.1:n.42+4168A=
XR_929758.1:n.63+4168A=
XR_929759.1:n.63+4168A=
XM_011518511.2:c.42+4168A=	XP_011516813.1:n.42+4168A=
XM_011518515.2:c.42+4168A=	XP_011516817.1:n.42+4168A=
XM_011518516.2:c.42+4168A=	XP_011516818.1:n.42+4168A=
XM_017014612.2:c.-16+11270A=	XP_016870101.1:n.-16+11270A=
XM_017014613.1:c.42+4168A=	XP_016870102.1:n.42+4168A=
XM_024447505.1:c.-347+4168A=	XP_024303273.1:n.-347+4168A=
XR_929758.3:n.573+4168A=