Canonical Allele Identifier: CA8980231

Gene: CCBE1

Linked Data

• dbSNP Id: rs757789723
• ExAC: 18:57105350 C / T
• gnomAD v2: 18-57105350-C-T
• gnomAD v4: 18-59438118-C-T
• MyVariant Identifiers: chr18:g.57105350C>T (hg19) ; chr18:g.59438118C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.59438118C>T , CM000680.2:g.59438118C>T	GRCh38
NC_000018.9:g.57105350C>T , CM000680.1:g.57105350C>T	GRCh37
NC_000018.8:g.55256330C>T	NCBI36
NG_016990.1:g.264295G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000589419.2:n.983G>A
ENST00000650467.2:c.758G>A	ENSP00000496897.2:p.Gly253Glu
ENST00000695903.1:c.1093G>A	ENSP00000512255.1:p.Gly365Ser
ENST00000695904.1:c.1093G>A	ENSP00000512259.1:p.Gly365Ser
ENST00000439986.9:c.980G>A MANE Select	ENSP00000404464.2:p.Gly327Glu
ENST00000589116.2:n.688G>A
ENST00000649564.1:c.980G>A	ENSP00000497183.1:p.Gly327Glu
ENST00000650467.1:c.636G>A
ENST00000398179.3:c.770G>A	ENSP00000381241.3:p.Gly257Glu
ENST00000439986.8:c.980G>A	ENSP00000404464.2:p.Gly327Glu
ENST00000589116.1:n.688G>A
NM_133459.3:c.980G>A	NP_597716.1:p.Gly327Glu
XM_005266648.2:c.980G>A	XP_005266705.1:p.Gly327Glu
NM_133459.4:c.980G>A MANE Select	NP_597716.1:p.Gly327Glu
XM_017025556.1:c.1093G>A	XP_016881045.1:p.Gly365Ser
XM_017025557.1:c.1093G>A	XP_016881046.1:p.Gly365Ser
XM_017025558.1:c.980G>A	XP_016881047.1:p.Gly327Glu
XM_024451091.1:c.980G>A	XP_024306859.1:p.Gly327Glu
XR_001753142.1:n.1932G>A