Canonical Allele Identifier: CA345673359
Gene: ZBTB18 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.244054411C>A , CM000663.2:g.244054411C>A GRCh38
NC_000001.10:g.244217713C>A , CM000663.1:g.244217713C>A GRCh37
NC_000001.9:g.242284336C>A NCBI36
NG_033841.1:g.10473C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696615.1:c.610C>A ENSP00000512755.1:p.His204Asn
ENST00000696616.1:c.610C>A ENSP00000512756.1:p.His204Asn
ENST00000696617.1:c.*567C>A ENSP00000512757.1:n.*567C>A
ENST00000696618.1:c.610C>A ENSP00000512758.1:p.His204Asn
ENST00000358704.4:c.637C>A MANE Select ENSP00000351539.4:p.His213Asn
ENST00000622512.1:c.610C>A ENSP00000481278.1:p.His204Asn
NM_001278196.1:c.610C>A NP_001265125.1:p.His204Asn
NM_006352.4:c.610C>A NP_006343.2:p.His204Asn
NM_205768.2:c.637C>A NP_991331.1:p.His213Asn
XM_005273006.2:c.610C>A XP_005273063.1:p.His204Asn
XM_017000060.1:c.610C>A XP_016855549.1:p.His204Asn
NM_001278196.2:c.610C>A NP_001265125.1:p.His204Asn
NM_205768.3:c.637C>A MANE Select NP_991331.1:p.His213Asn