Canonical Allele Identifier: CA1845926610

Gene: UNC13B

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35271739T= , CM000671.2:g.35271739T=	GRCh38
NC_000009.11:g.35271736T= , CM000671.1:g.35271736T=	GRCh37
NC_000009.10:g.35261736T=	NCBI36
NG_033014.1:g.114748T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000635942.2:c.526+12689T= MANE Select	ENSP00000490228.1:n.526+12689T=
ENST00000635942.1:c.526+12689T=	ENSP00000490228.1:n.526+12689T=
ENST00000378495.7:c.526+12689T=	ENSP00000367756.3:n.526+12689T=
ENST00000378496.8:c.-743+12689T=	ENSP00000367757.5:n.-743+12689T=
ENST00000396787.5:c.526+12689T=	ENSP00000380006.1:n.526+12689T=
ENST00000617908.4:c.-720+12689T=	ENSP00000484432.1:n.-720+12689T=
ENST00000619578.4:c.526+12689T=	ENSP00000479261.1:n.526+12689T=
ENST00000634487.1:c.526+12689T=	ENSP00000489581.1:n.526+12689T=
NM_006377.3:c.526+12689T=	NP_006368.3:n.526+12689T=
XM_011517684.1:c.526+12689T=	XP_011515986.1:n.526+12689T=
XM_011517685.1:c.526+12689T=	XP_011515987.1:n.526+12689T=
NM_001330653.1:c.526+12689T=	NP_001317582.1:n.526+12689T=
XM_011517685.3:c.526+12689T=	XP_011515987.1:n.526+12689T=
NM_001330653.2:c.526+12689T=	NP_001317582.1:n.526+12689T=
NM_001371186.1:c.526+12689T=	NP_001358115.1:n.526+12689T=
NM_001371189.1:c.526+12689T=	NP_001358118.1:n.526+12689T=
NM_006377.5:c.526+12689T=	NP_006368.3:n.526+12689T=
NM_001330653.3:c.526+12689T=	NP_001317582.1:n.526+12689T=
NM_001371186.2:c.526+12689T=	NP_001358115.1:n.526+12689T=
NM_001371189.2:c.526+12689T= MANE Select	NP_001358118.1:n.526+12689T=
NM_001387551.1:c.526+12689T=	NP_001374480.1:n.526+12689T=
NM_001387553.1:c.379+12689T=	NP_001374482.1:n.379+12689T=
NM_001387554.1:c.379+12689T=	NP_001374483.1:n.379+12689T=
NM_006377.6:c.526+12689T=	NP_006368.3:n.526+12689T=
NR_170667.1:n.801+12689T=