Canonical Allele Identifier: CA345674065

Gene: ZBTB18

Linked Data

• MyVariant Identifiers: chr1:g.244218032A>T (hg19) ; chr1:g.244054730A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244054730A>T , CM000663.2:g.244054730A>T	GRCh38
NC_000001.10:g.244218032A>T , CM000663.1:g.244218032A>T	GRCh37
NC_000001.9:g.242284655A>T	NCBI36
NG_033841.1:g.10792A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000696615.1:c.*133A>T	ENSP00000512755.1:n.*133A>T
ENST00000696616.1:c.929A>T	ENSP00000512756.1:p.Glu310Val
ENST00000696617.1:c.*886A>T	ENSP00000512757.1:n.*886A>T
ENST00000696618.1:c.929A>T	ENSP00000512758.1:p.Glu310Val
ENST00000358704.4:c.956A>T MANE Select	ENSP00000351539.4:p.Glu319Val
ENST00000622512.1:c.929A>T	ENSP00000481278.1:p.Glu310Val
NM_001278196.1:c.929A>T	NP_001265125.1:p.Glu310Val
NM_006352.4:c.929A>T	NP_006343.2:p.Glu310Val
NM_205768.2:c.956A>T	NP_991331.1:p.Glu319Val
XM_005273006.2:c.929A>T	XP_005273063.1:p.Glu310Val
XM_017000060.1:c.929A>T	XP_016855549.1:p.Glu310Val
NM_001278196.2:c.929A>T	NP_001265125.1:p.Glu310Val
NM_205768.3:c.956A>T MANE Select	NP_991331.1:p.Glu319Val