Canonical Allele Identifier: CA93702519
Gene: CCKAR HGNC NCBI

Linked Data

dbSNP Id: rs756797239
gnomAD v2: 4-26491753-T-G
gnomAD v4: 4-26490131-T-G
MyVariant Identifiers: chr4:g.26491753T>G (hg19) chr4:g.26490131T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26490131T>G , CM000666.2:g.26490131T>G GRCh38
NC_000004.11:g.26491753T>G , CM000666.1:g.26491753T>G GRCh37
NC_000004.10:g.26100851T>G NCBI36
NG_012053.1:g.5290A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000295589.4:c.112+25A>C MANE Select ENSP00000295589.3:n.112+25A>C
ENST00000295589.3:c.112+25A>C ENSP00000295589.3:n.112+25A>C
NM_000730.2:c.112+25A>C NP_000721.1:n.112+25A>C
NM_000730.3:c.112+25A>C MANE Select NP_000721.1:n.112+25A>C
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