Canonical Allele Identifier: CA93702500
Gene: CCKAR HGNC NCBI

Linked Data

dbSNP Id: rs566326463
gnomAD v2: 4-26491690-A-G
gnomAD v3: 4-26490068-A-G
gnomAD v4: 4-26490068-A-G
MyVariant Identifiers: chr4:g.26491690A>G (hg19) chr4:g.26490068A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26490068A>G , CM000666.2:g.26490068A>G GRCh38
NC_000004.11:g.26491690A>G , CM000666.1:g.26491690A>G GRCh37
NC_000004.10:g.26100788A>G NCBI36
NG_012053.1:g.5353T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000295589.4:c.112+88T>C MANE Select ENSP00000295589.3:n.112+88T>C
ENST00000295589.3:c.112+88T>C ENSP00000295589.3:n.112+88T>C
NM_000730.2:c.112+88T>C NP_000721.1:n.112+88T>C
NM_000730.3:c.112+88T>C MANE Select NP_000721.1:n.112+88T>C
Search 100 bp 5'
Search 100 bp 3'