Canonical Allele Identifier: CA15152636

Gene: EFR3B

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25082887C>T , CM000664.2:g.25082887C>T	GRCh38
NC_000002.11:g.25305756C>T , CM000664.1:g.25305756C>T	GRCh37
NC_000002.10:g.25159260C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403714.8:c.8-8438C>T MANE Select	ENSP00000384081.3:n.8-8438C>T
ENST00000401432.7:c.8-8438C>T	ENSP00000386082.3:n.8-8438C>T
ENST00000402191.5:c.-98-8438C>T	ENSP00000385832.1:n.-98-8438C>T
ENST00000403714.7:c.8-8438C>T	ENSP00000384081.3:n.8-8438C>T
NM_014971.1:c.8-8438C>T	NP_055786.1:n.8-8438C>T
XM_011532701.1:c.8-8438C>T	XP_011531003.1:n.8-8438C>T
XM_011532702.1:c.88-8438C>T	XP_011531004.1:n.88-8438C>T
XM_011532703.1:c.-98-8438C>T	XP_011531005.1:n.-98-8438C>T
NM_001319099.1:c.-98-8438C>T	NP_001306028.1:n.-98-8438C>T
XM_011532701.3:c.8-8438C>T	XP_011531003.1:n.8-8438C>T
XR_001738675.2:n.78-8438C>T
NM_014971.2:c.8-8438C>T MANE Select	NP_055786.1:n.8-8438C>T
NM_001319099.2:c.-98-8438C>T	NP_001306028.1:n.-98-8438C>T