Canonical Allele Identifier: CA424410882

Gene: ZBTB18

Linked Data

• MyVariant Identifiers: chr1:g.244217742C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244054440C>A , CM000663.2:g.244054440C>A	GRCh38
NC_000001.10:g.244217742C>A , CM000663.1:g.244217742C>A	GRCh37
NC_000001.9:g.242284365C>A	NCBI36
NG_033841.1:g.10502C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696615.1:c.639C>A	ENSP00000512755.1:p.Ala213=
ENST00000696616.1:c.639C>A	ENSP00000512756.1:p.Ala213=
ENST00000696617.1:c.*596C>A	ENSP00000512757.1:n.*596C>A
ENST00000696618.1:c.639C>A	ENSP00000512758.1:p.Ala213=
ENST00000358704.4:c.666C>A MANE Select	ENSP00000351539.4:p.Ala222=
ENST00000622512.1:c.639C>A	ENSP00000481278.1:p.Ala213=
NM_001278196.1:c.639C>A	NP_001265125.1:p.Ala213=
NM_006352.4:c.639C>A	NP_006343.2:p.Ala213=
NM_205768.2:c.666C>A	NP_991331.1:p.Ala222=
XM_005273006.2:c.639C>A	XP_005273063.1:p.Ala213=
XM_017000060.1:c.639C>A	XP_016855549.1:p.Ala213=
NM_001278196.2:c.639C>A	NP_001265125.1:p.Ala213=
NM_205768.3:c.666C>A MANE Select	NP_991331.1:p.Ala222=