Canonical Allele Identifier: CA93699973

Gene: CCKAR

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.26484660A>G , CM000666.2:g.26484660A>G	GRCh38
NC_000004.11:g.26486282A>G , CM000666.1:g.26486282A>G	GRCh37
NC_000004.10:g.26095380A>G	NCBI36
NG_012053.1:g.10761T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295589.4:c.626+977T>C MANE Select	ENSP00000295589.3:n.626+977T>C
ENST00000295589.3:c.626+977T>C	ENSP00000295589.3:n.626+977T>C
NM_000730.2:c.626+977T>C	NP_000721.1:n.626+977T>C
NM_000730.3:c.626+977T>C MANE Select	NP_000721.1:n.626+977T>C