Canonical Allele Identifier: CA1845924566

Gene: UNC13B

Linked Data

• dbSNP Id: rs10121009

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35269822T>G , CM000671.2:g.35269822T>G	GRCh38
NC_000009.11:g.35269819T>G , CM000671.1:g.35269819T>G	GRCh37
NC_000009.10:g.35259819T>G	NCBI36
NG_033014.1:g.112831T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000635942.2:c.526+10772T>G MANE Select	ENSP00000490228.1:n.526+10772T>G
ENST00000635942.1:c.526+10772T>G	ENSP00000490228.1:n.526+10772T>G
ENST00000378495.7:c.526+10772T>G	ENSP00000367756.3:n.526+10772T>G
ENST00000378496.8:c.-743+10772T>G	ENSP00000367757.5:n.-743+10772T>G
ENST00000396787.5:c.526+10772T>G	ENSP00000380006.1:n.526+10772T>G
ENST00000617908.4:c.-720+10772T>G	ENSP00000484432.1:n.-720+10772T>G
ENST00000619578.4:c.526+10772T>G	ENSP00000479261.1:n.526+10772T>G
ENST00000634487.1:c.526+10772T>G	ENSP00000489581.1:n.526+10772T>G
NM_006377.3:c.526+10772T>G	NP_006368.3:n.526+10772T>G
XM_011517684.1:c.526+10772T>G	XP_011515986.1:n.526+10772T>G
XM_011517685.1:c.526+10772T>G	XP_011515987.1:n.526+10772T>G
NM_001330653.1:c.526+10772T>G	NP_001317582.1:n.526+10772T>G
XM_011517685.3:c.526+10772T>G	XP_011515987.1:n.526+10772T>G
NM_001330653.2:c.526+10772T>G	NP_001317582.1:n.526+10772T>G
NM_001371186.1:c.526+10772T>G	NP_001358115.1:n.526+10772T>G
NM_001371189.1:c.526+10772T>G	NP_001358118.1:n.526+10772T>G
NM_006377.5:c.526+10772T>G	NP_006368.3:n.526+10772T>G
NM_001330653.3:c.526+10772T>G	NP_001317582.1:n.526+10772T>G
NM_001371186.2:c.526+10772T>G	NP_001358115.1:n.526+10772T>G
NM_001371189.2:c.526+10772T>G MANE Select	NP_001358118.1:n.526+10772T>G
NM_001387551.1:c.526+10772T>G	NP_001374480.1:n.526+10772T>G
NM_001387553.1:c.379+10772T>G	NP_001374482.1:n.379+10772T>G
NM_001387554.1:c.379+10772T>G	NP_001374483.1:n.379+10772T>G
NM_006377.6:c.526+10772T>G	NP_006368.3:n.526+10772T>G
NR_170667.1:n.801+10772T>G