Canonical Allele Identifier: CA2881921
Gene: CCKAR HGNC NCBI

Linked Data

dbSNP Id: rs200910008
ExAC: 4:26491732 C / T
gnomAD v2: 4-26491732-C-T
gnomAD v4: 4-26490110-C-T
MyVariant Identifiers: chr4:g.26491732C>T (hg19) chr4:g.26490110C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26490110C>T , CM000666.2:g.26490110C>T GRCh38
NC_000004.11:g.26491732C>T , CM000666.1:g.26491732C>T GRCh37
NC_000004.10:g.26100830C>T NCBI36
NG_012053.1:g.5311G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000295589.4:c.112+46G>A MANE Select ENSP00000295589.3:n.112+46G>A
ENST00000295589.3:c.112+46G>A ENSP00000295589.3:n.112+46G>A
NM_000730.2:c.112+46G>A NP_000721.1:n.112+46G>A
NM_000730.3:c.112+46G>A MANE Select NP_000721.1:n.112+46G>A
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