Canonical Allele Identifier: CA424411164

Gene: ZBTB18

Linked Data

• MyVariant Identifiers: chr1:g.244218024A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244054722A>C , CM000663.2:g.244054722A>C	GRCh38
NC_000001.10:g.244218024A>C , CM000663.1:g.244218024A>C	GRCh37
NC_000001.9:g.242284647A>C	NCBI36
NG_033841.1:g.10784A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000696615.1:c.*125A>C	ENSP00000512755.1:n.*125A>C
ENST00000696616.1:c.921A>C	ENSP00000512756.1:p.Val307=
ENST00000696617.1:c.*878A>C	ENSP00000512757.1:n.*878A>C
ENST00000696618.1:c.921A>C	ENSP00000512758.1:p.Val307=
ENST00000358704.4:c.948A>C MANE Select	ENSP00000351539.4:p.Val316=
ENST00000622512.1:c.921A>C	ENSP00000481278.1:p.Val307=
NM_001278196.1:c.921A>C	NP_001265125.1:p.Val307=
NM_006352.4:c.921A>C	NP_006343.2:p.Val307=
NM_205768.2:c.948A>C	NP_991331.1:p.Val316=
XM_005273006.2:c.921A>C	XP_005273063.1:p.Val307=
XM_017000060.1:c.921A>C	XP_016855549.1:p.Val307=
NM_001278196.2:c.921A>C	NP_001265125.1:p.Val307=
NM_205768.3:c.948A>C MANE Select	NP_991331.1:p.Val316=