Canonical Allele Identifier: CA2670266589
Gene: CCKAR HGNC NCBI

Linked Data

gnomAD v4: 4-26490141-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26490141G>A , CM000666.2:g.26490141G>A GRCh38
NC_000004.11:g.26491763G>A , CM000666.1:g.26491763G>A GRCh37
NC_000004.10:g.26100861G>A NCBI36
NG_012053.1:g.5280C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000295589.4:c.112+15C>T MANE Select ENSP00000295589.3:n.112+15C>T
ENST00000295589.3:c.112+15C>T ENSP00000295589.3:n.112+15C>T
NM_000730.2:c.112+15C>T NP_000721.1:n.112+15C>T
NM_000730.3:c.112+15C>T MANE Select NP_000721.1:n.112+15C>T
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