Canonical Allele Identifier: CA587561310

Gene: UNC13B

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35166766G>A , CM000671.2:g.35166766G>A	GRCh38
NC_000009.11:g.35166763G>A , CM000671.1:g.35166763G>A	GRCh37
NC_000009.10:g.35156763G>A	NCBI36
NG_033014.1:g.9775G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000635942.2:c.22+4461G>A MANE Select	ENSP00000490228.1:n.22+4461G>A
ENST00000635942.1:c.22+4461G>A	ENSP00000490228.1:n.22+4461G>A
ENST00000378495.7:c.22+4461G>A	ENSP00000367756.3:n.22+4461G>A
ENST00000378496.8:c.-1247+4461G>A	ENSP00000367757.5:n.-1247+4461G>A
ENST00000396787.5:c.22+4461G>A	ENSP00000380006.1:n.22+4461G>A
ENST00000617908.4:c.-1224+4461G>A	ENSP00000484432.1:n.-1224+4461G>A
ENST00000619578.4:c.22+4461G>A	ENSP00000479261.1:n.22+4461G>A
ENST00000634487.1:c.22+4461G>A	ENSP00000489581.1:n.22+4461G>A
NM_006377.3:c.22+4461G>A	NP_006368.3:n.22+4461G>A
XM_011517684.1:c.22+4461G>A	XP_011515986.1:n.22+4461G>A
XM_011517685.1:c.22+4461G>A	XP_011515987.1:n.22+4461G>A
NM_001330653.1:c.22+4461G>A	NP_001317582.1:n.22+4461G>A
XM_011517685.3:c.22+4461G>A	XP_011515987.1:n.22+4461G>A
NM_001330653.2:c.22+4461G>A	NP_001317582.1:n.22+4461G>A
NM_001371186.1:c.22+4461G>A	NP_001358115.1:n.22+4461G>A
NM_001371189.1:c.22+4461G>A	NP_001358118.1:n.22+4461G>A
NM_006377.5:c.22+4461G>A	NP_006368.3:n.22+4461G>A
NM_001330653.3:c.22+4461G>A	NP_001317582.1:n.22+4461G>A
NM_001371186.2:c.22+4461G>A	NP_001358115.1:n.22+4461G>A
NM_001371189.2:c.22+4461G>A MANE Select	NP_001358118.1:n.22+4461G>A
NM_001387551.1:c.22+4461G>A	NP_001374480.1:n.22+4461G>A
NM_006377.6:c.22+4461G>A	NP_006368.3:n.22+4461G>A
NR_170667.1:n.297+4461G>A