Canonical Allele Identifier: CA1230659729

Gene: ZBTB18

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244054398A= , CM000663.2:g.244054398A=	GRCh38
NC_000001.10:g.244217700A= , CM000663.1:g.244217700A=	GRCh37
NC_000001.9:g.242284323A=	NCBI36
NG_033841.1:g.10460A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696615.1:c.597A=	ENSP00000512755.1:p.Gly199=
ENST00000696616.1:c.597A=	ENSP00000512756.1:p.Gly199=
ENST00000696617.1:c.*554A=	ENSP00000512757.1:n.*554A=
ENST00000696618.1:c.597A=	ENSP00000512758.1:p.Gly199=
ENST00000358704.4:c.624A= MANE Select	ENSP00000351539.4:p.Gly208=
ENST00000622512.1:c.597A=	ENSP00000481278.1:p.Gly199=
NM_001278196.1:c.597A=	NP_001265125.1:p.Gly199=
NM_006352.4:c.597A=	NP_006343.2:p.Gly199=
NM_205768.2:c.624A=	NP_991331.1:p.Gly208=
XM_005273006.2:c.597A=	XP_005273063.1:p.Gly199=
XM_017000060.1:c.597A=	XP_016855549.1:p.Gly199=
NM_001278196.2:c.597A=	NP_001265125.1:p.Gly199=
NM_205768.3:c.624A= MANE Select	NP_991331.1:p.Gly208=