Canonical Allele Identifier: CA93702509
Gene: CCKAR HGNC NCBI

Linked Data

dbSNP Id: rs201415344
gnomAD v4: 4-26490119-A-C
MyVariant Identifiers: chr4:g.26491741A>C (hg19) chr4:g.26490119A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26490119A>C , CM000666.2:g.26490119A>C GRCh38
NC_000004.11:g.26491741A>C , CM000666.1:g.26491741A>C GRCh37
NC_000004.10:g.26100839A>C NCBI36
NG_012053.1:g.5302T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000295589.4:c.112+37T>G MANE Select ENSP00000295589.3:n.112+37T>G
ENST00000295589.3:c.112+37T>G ENSP00000295589.3:n.112+37T>G
NM_000730.2:c.112+37T>G NP_000721.1:n.112+37T>G
NM_000730.3:c.112+37T>G MANE Select NP_000721.1:n.112+37T>G
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