Canonical Allele Identifier: CA2881924
Gene: CCKAR HGNC NCBI

Linked Data

dbSNP Id: rs774176022
ExAC: 4:26491742 G / A
gnomAD v2: 4-26491742-G-A
gnomAD v4: 4-26490120-G-A
MyVariant Identifiers: chr4:g.26491742G>A (hg19) chr4:g.26490120G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26490120G>A , CM000666.2:g.26490120G>A GRCh38
NC_000004.11:g.26491742G>A , CM000666.1:g.26491742G>A GRCh37
NC_000004.10:g.26100840G>A NCBI36
NG_012053.1:g.5301C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000295589.4:c.112+36C>T MANE Select ENSP00000295589.3:n.112+36C>T
ENST00000295589.3:c.112+36C>T ENSP00000295589.3:n.112+36C>T
NM_000730.2:c.112+36C>T NP_000721.1:n.112+36C>T
NM_000730.3:c.112+36C>T MANE Select NP_000721.1:n.112+36C>T
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