Canonical Allele Identifier: CA645586294

Gene: CCKBR

Linked Data

• dbSNP Id: rs1800843
• gnomAD v3: 11-6270835-C-T
• gnomAD v4: 11-6270835-C-T
• COSMIC: COSM3952853

Genomic Alleles

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

Transcript Alleles

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