Canonical Allele Identifier: CA424410963

Gene: ZBTB18

Linked Data

• gnomAD v4: 1-244054470-C-G
• MyVariant Identifiers: chr1:g.244217772C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244054470C>G , CM000663.2:g.244054470C>G	GRCh38
NC_000001.10:g.244217772C>G , CM000663.1:g.244217772C>G	GRCh37
NC_000001.9:g.242284395C>G	NCBI36
NG_033841.1:g.10532C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696615.1:c.669C>G	ENSP00000512755.1:p.Ser223=
ENST00000696616.1:c.669C>G	ENSP00000512756.1:p.Ser223=
ENST00000696617.1:c.*626C>G	ENSP00000512757.1:n.*626C>G
ENST00000696618.1:c.669C>G	ENSP00000512758.1:p.Ser223=
ENST00000358704.4:c.696C>G MANE Select	ENSP00000351539.4:p.Ser232=
ENST00000622512.1:c.669C>G	ENSP00000481278.1:p.Ser223=
NM_001278196.1:c.669C>G	NP_001265125.1:p.Ser223=
NM_006352.4:c.669C>G	NP_006343.2:p.Ser223=
NM_205768.2:c.696C>G	NP_991331.1:p.Ser232=
XM_005273006.2:c.669C>G	XP_005273063.1:p.Ser223=
XM_017000060.1:c.669C>G	XP_016855549.1:p.Ser223=
NM_001278196.2:c.669C>G	NP_001265125.1:p.Ser223=
NM_205768.3:c.696C>G MANE Select	NP_991331.1:p.Ser232=