Canonical Allele Identifier: CA2578103145
Gene: CCKAR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26490109A>G , CM000666.2:g.26490109A>G GRCh38
NC_000004.11:g.26491731A>G , CM000666.1:g.26491731A>G GRCh37
NC_000004.10:g.26100829A>G NCBI36
NG_012053.1:g.5312T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000295589.4:c.112+47T>C MANE Select ENSP00000295589.3:n.112+47T>C
ENST00000295589.3:c.112+47T>C ENSP00000295589.3:n.112+47T>C
NM_000730.2:c.112+47T>C NP_000721.1:n.112+47T>C
NM_000730.3:c.112+47T>C MANE Select NP_000721.1:n.112+47T>C