Canonical Allele Identifier: CA8040938

Gene: PHKB

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.47649097C>T , CM000678.2:g.47649097C>T	GRCh38
NC_000016.9:g.47683008C>T , CM000678.1:g.47683008C>T	GRCh37
NC_000016.8:g.46240509C>T	NCBI36
NG_016598.1:g.192799C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000293.3:c.1693-3C>T MANE Select	NP_000284.1:n.1693-3C>T
ENST00000323584.10:c.1693-3C>T MANE Select	ENSP00000313504.5:n.1693-3C>T
NM_000293.2:c.1693-3C>T	NP_000284.1:n.1693-3C>T
NM_001031835.2:c.1672-3C>T	NP_001027005.1:n.1672-3C>T
NM_001031835.3:c.1672-3C>T	NP_001027005.1:n.1672-3C>T
NM_001363837.1:c.1693-3C>T	NP_001350766.1:n.1693-3C>T
ENST00000299167.12:c.1693-3C>T	ENSP00000299167.8:n.1693-3C>T
ENST00000323584.9:c.1693-3C>T	ENSP00000313504.5:n.1693-3C>T
ENST00000566044.5:c.1672-3C>T	ENSP00000456729.1:n.1672-3C>T
ENST00000696809.1:c.*267-3C>T	ENSP00000512887.1:n.*267-3C>T
ENST00000699276.1:c.1672-3C>T	ENSP00000514257.1:n.1672-3C>T
XM_005255983.3:c.1693-3C>T	XP_005256040.1:n.1693-3C>T
XM_005255983.4:c.1693-3C>T	XP_005256040.1:n.1693-3C>T
XM_005255984.3:c.1672-3C>T	XP_005256041.1:n.1672-3C>T
XM_005255984.4:c.1672-3C>T	XP_005256041.1:n.1672-3C>T
XM_011523106.1:c.1693-3C>T	XP_011521408.1:n.1693-3C>T
XM_011523107.1:c.271-3C>T	XP_011521409.1:n.271-3C>T
XM_017023282.1:c.580-3C>T	XP_016878771.1:n.580-3C>T
XM_017023283.1:c.271-3C>T	XP_016878772.1:n.271-3C>T
XM_017023284.1:c.271-3C>T	XP_016878773.1:n.271-3C>T
XR_001751913.1:n.1708-3C>T