Canonical Allele Identifier: CA44265042

Gene: EFR3B

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25053415G>A , CM000664.2:g.25053415G>A	GRCh38
NC_000002.11:g.25276284G>A , CM000664.1:g.25276284G>A	GRCh37
NC_000002.10:g.25129788G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403714.8:c.7+11096G>A MANE Select	ENSP00000384081.3:n.7+11096G>A
ENST00000401432.7:c.7+11096G>A	ENSP00000386082.3:n.7+11096G>A
ENST00000402191.5:c.-99+10749G>A	ENSP00000385832.1:n.-99+10749G>A
ENST00000403714.7:c.7+11096G>A	ENSP00000384081.3:n.7+11096G>A
NM_014971.1:c.7+11096G>A	NP_055786.1:n.7+11096G>A
XM_011532701.1:c.7+11096G>A	XP_011531003.1:n.7+11096G>A
XM_011532702.1:c.87+11096G>A	XP_011531004.1:n.87+11096G>A
XM_011532703.1:c.-99+10749G>A	XP_011531005.1:n.-99+10749G>A
NM_001319099.1:c.-99+10749G>A	NP_001306028.1:n.-99+10749G>A
XM_011532701.3:c.7+11096G>A	XP_011531003.1:n.7+11096G>A
XR_001738675.2:n.77+11096G>A
NM_014971.2:c.7+11096G>A MANE Select	NP_055786.1:n.7+11096G>A
NM_001319099.2:c.-99+10749G>A	NP_001306028.1:n.-99+10749G>A