Canonical Allele Identifier: CA2578103146
Gene: CCKAR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26490115C>G , CM000666.2:g.26490115C>G GRCh38
NC_000004.11:g.26491737C>G , CM000666.1:g.26491737C>G GRCh37
NC_000004.10:g.26100835C>G NCBI36
NG_012053.1:g.5306G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000295589.4:c.112+41G>C MANE Select ENSP00000295589.3:n.112+41G>C
ENST00000295589.3:c.112+41G>C ENSP00000295589.3:n.112+41G>C
NM_000730.2:c.112+41G>C NP_000721.1:n.112+41G>C
NM_000730.3:c.112+41G>C MANE Select NP_000721.1:n.112+41G>C
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