Canonical Allele Identifier: CA424410776

Gene: ZBTB18

Linked Data

• MyVariant Identifiers: chr1:g.244217697C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244054395C>G , CM000663.2:g.244054395C>G	GRCh38
NC_000001.10:g.244217697C>G , CM000663.1:g.244217697C>G	GRCh37
NC_000001.9:g.242284320C>G	NCBI36
NG_033841.1:g.10457C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696615.1:c.594C>G	ENSP00000512755.1:p.Gly198=
ENST00000696616.1:c.594C>G	ENSP00000512756.1:p.Gly198=
ENST00000696617.1:c.*551C>G	ENSP00000512757.1:n.*551C>G
ENST00000696618.1:c.594C>G	ENSP00000512758.1:p.Gly198=
ENST00000358704.4:c.621C>G MANE Select	ENSP00000351539.4:p.Gly207=
ENST00000622512.1:c.594C>G	ENSP00000481278.1:p.Gly198=
NM_001278196.1:c.594C>G	NP_001265125.1:p.Gly198=
NM_006352.4:c.594C>G	NP_006343.2:p.Gly198=
NM_205768.2:c.621C>G	NP_991331.1:p.Gly207=
XM_005273006.2:c.594C>G	XP_005273063.1:p.Gly198=
XM_017000060.1:c.594C>G	XP_016855549.1:p.Gly198=
NM_001278196.2:c.594C>G	NP_001265125.1:p.Gly198=
NM_205768.3:c.621C>G MANE Select	NP_991331.1:p.Gly207=