Canonical Allele Identifier: CA1708304

Gene: EXOC6B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.72379881A>G , CM000664.2:g.72379881A>G	GRCh38
NC_000002.11:g.72607010A>G , CM000664.1:g.72607010A>G	GRCh37
NC_000002.10:g.72460518A>G	NCBI36
NG_050967.1:g.451168T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_015189.3:c.1981-11T>C MANE Select	NP_056004.1:n.1981-11T>C
ENST00000272427.11:c.1981-11T>C MANE Select	ENSP00000272427.7:n.1981-11T>C
NM_001321729.1:c.1981-11T>C	NP_001308658.1:n.1981-11T>C
NM_001321729.2:c.1981-11T>C	NP_001308658.1:n.1981-11T>C
NM_001321730.1:c.1846-11T>C	NP_001308659.1:n.1846-11T>C
NM_001321730.2:c.1846-11T>C	NP_001308659.1:n.1846-11T>C
NM_001321731.1:c.1981-11T>C	NP_001308660.1:n.1981-11T>C
NM_001321731.2:c.1981-11T>C	NP_001308660.1:n.1981-11T>C
NM_001321733.1:c.1846-11T>C	NP_001308662.1:n.1846-11T>C
NM_001321733.2:c.1846-11T>C	NP_001308662.1:n.1846-11T>C
NM_001321734.1:c.1642-11T>C	NP_001308663.1:n.1642-11T>C
NM_001321734.2:c.1642-11T>C	NP_001308663.1:n.1642-11T>C
NM_015189.1:c.1981-11T>C	NP_056004.1:n.1981-11T>C
NM_015189.2:c.1981-11T>C	NP_056004.1:n.1981-11T>C
NR_135773.1:n.2113-11T>C
NR_135773.2:n.2104-11T>C
NR_135774.1:n.1933-44861T>C
NR_135774.2:n.1924-44861T>C
ENST00000272427.10:c.1981-11T>C	ENSP00000272427.6:n.1981-11T>C
ENST00000464347.2:n.403-11T>C
ENST00000634650.1:c.1981-11T>C	ENSP00000489442.1:n.1981-11T>C
XM_005264223.1:c.1981-11T>C	XP_005264280.1:n.1981-11T>C
XM_005264224.1:c.985-11T>C	XP_005264281.1:n.985-11T>C
XM_011532710.1:c.1912-11T>C	XP_011531012.1:n.1912-11T>C
XM_017003641.1:c.1435-11T>C	XP_016859130.1:n.1435-11T>C
XM_017003642.1:c.985-11T>C	XP_016859131.1:n.985-11T>C