Canonical Allele Identifier: CA2760810553
Gene: CCKAR HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26490021T>C , CM000666.2:g.26490021T>C GRCh38
NC_000004.11:g.26491643T>C , CM000666.1:g.26491643T>C GRCh37
NC_000004.10:g.26100741T>C NCBI36
NG_012053.1:g.5400A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000295589.4:c.112+135A>G MANE Select ENSP00000295589.3:n.112+135A>G
ENST00000295589.3:c.112+135A>G ENSP00000295589.3:n.112+135A>G
NM_000730.2:c.112+135A>G NP_000721.1:n.112+135A>G
NM_000730.3:c.112+135A>G MANE Select NP_000721.1:n.112+135A>G
Search 100 bp 5'
Search 100 bp 3'