Canonical Allele Identifier: CA2670266591
Gene: CCKAR HGNC NCBI

Linked Data

gnomAD v4: 4-26490144-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26490144T>C , CM000666.2:g.26490144T>C GRCh38
NC_000004.11:g.26491766T>C , CM000666.1:g.26491766T>C GRCh37
NC_000004.10:g.26100864T>C NCBI36
NG_012053.1:g.5277A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000295589.4:c.112+12A>G MANE Select ENSP00000295589.3:n.112+12A>G
ENST00000295589.3:c.112+12A>G ENSP00000295589.3:n.112+12A>G
NM_000730.2:c.112+12A>G NP_000721.1:n.112+12A>G
NM_000730.3:c.112+12A>G MANE Select NP_000721.1:n.112+12A>G
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