Canonical Allele Identifier: CA15685074

Gene: POU2AF1 BTG4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.111404408G>A , CM000673.2:g.111404408G>A	GRCh38
NC_000011.9:g.111275133G>A , CM000673.1:g.111275133G>A	GRCh37
NC_000011.8:g.110780343G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000515029.2:n.155+213C>T (POU2AF1)
ENST00000531398.1:c.22+213C>T (POU2AF1)	ENSP00000433527.1:n.22+213C>T
XM_011542876.1:c.764+213C>T (BTG4)	XP_011541178.1:n.764+213C>T
XM_011542878.1:c.768+209C>T (BTG4)	XP_011541180.1:n.768+209C>T
XR_947832.1:n.998+213C>T (BTG4)
XR_947833.1:n.998+213C>T (BTG4)
XR_947834.1:n.998+213C>T (BTG4)
XR_947835.1:n.998+213C>T (BTG4)
XR_947836.1:n.998+213C>T (BTG4)
XR_947837.1:n.1082+213C>T (BTG4)
XR_947838.1:n.857+213C>T (BTG4)
XR_947839.1:n.1095+213C>T (BTG4)
XR_947840.1:n.908+213C>T (BTG4)
XR_947841.1:n.950+213C>T (BTG4)
XR_947842.1:n.814+213C>T (BTG4)
XR_947843.1:n.998+213C>T (BTG4)
XR_947844.1:n.998+213C>T (BTG4)
XR_947845.1:n.998+213C>T (BTG4)
XR_947846.1:n.998+213C>T (BTG4)
XR_947848.1:n.998+213C>T (BTG4)
XR_947849.1:n.998+213C>T (BTG4)
XR_947850.1:n.1002+209C>T (BTG4)
XR_947851.1:n.1002+209C>T (BTG4)
XR_947852.1:n.1002+209C>T (BTG4)
XR_947853.1:n.967+213C>T (BTG4)
XM_011542876.2:c.764+213C>T (BTG4)	XP_011541178.1:n.764+213C>T
XM_011542878.3:c.768+209C>T (BTG4)	XP_011541180.1:n.768+209C>T
XM_024448587.1:c.764+213C>T (BTG4)	XP_024304355.1:n.764+213C>T
XM_024448588.1:c.764+213C>T (BTG4)	XP_024304356.1:n.764+213C>T
XM_024448589.1:c.764+213C>T (BTG4)	XP_024304357.1:n.764+213C>T
XM_024448590.1:c.764+213C>T (BTG4)	XP_024304358.1:n.764+213C>T
XM_024448591.1:c.764+213C>T (BTG4)	XP_024304359.1:n.764+213C>T
XM_024448592.1:c.662+213C>T (BTG4)	XP_024304360.1:n.662+213C>T
XR_947834.2:n.998+213C>T (BTG4)
XR_947835.2:n.998+213C>T (BTG4)
XR_947848.2:n.998+213C>T (BTG4)
XR_947849.2:n.998+213C>T (BTG4)
XR_947851.2:n.1002+209C>T (BTG4)
XR_947852.2:n.1002+209C>T (BTG4)