Canonical Allele Identifier: CA5851971

Gene: CCKBR

Linked Data

• dbSNP Id: rs1800843
• ExAC: 11:6292065 C / G
• gnomAD v4: 11-6270835-C-G
• MyVariant Identifiers: chr11:g.6292065C>G (hg19) ; chr11:g.6270835C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6270835C>G , CM000673.2:g.6270835C>G	GRCh38
NC_000011.9:g.6292065C>G , CM000673.1:g.6292065C>G	GRCh37
NC_000011.8:g.6248641C>G	NCBI36
NG_030591.1:g.16162C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000334619.7:c.811+32C>G MANE Select	ENSP00000335544.2:n.811+32C>G
ENST00000334619.6:c.811+32C>G	ENSP00000335544.2:n.811+32C>G
ENST00000525462.1:c.843C>G	ENSP00000435534.1:p.Gly281=
ENST00000532396.1:n.43+17C>G
ENST00000532715.5:c.559+32C>G	ENSP00000432079.1:n.559+32C>G
NM_176875.3:c.811+32C>G	NP_795344.1:n.811+32C>G
XM_005253210.1:c.843C>G	XP_005253267.1:p.Gly281=
XM_011520443.1:c.613+32C>G	XP_011518745.1:n.613+32C>G
NM_001318029.1:c.559+32C>G	NP_001304958.1:n.559+32C>G
NM_001363552.1:c.843C>G	NP_001350481.1:p.Gly281=
XM_017018516.1:c.613+32C>G	XP_016874005.1:n.613+32C>G
NM_176875.4:c.811+32C>G MANE Select	NP_795344.1:n.811+32C>G
NM_001318029.2:c.559+32C>G	NP_001304958.1:n.559+32C>G
NM_001363552.2:c.843C>G	NP_001350481.1:p.Gly281=