Canonical Allele Identifier: CA5059686

Gene: ZBTB5

Linked Data

• ClinVar Variation Id: 2513966
• ClinVar RCV Id: RCV004293469
• dbSNP Id: rs541667157
• ExAC: 9:37442181 G / A
• gnomAD v2: 9-37442181-G-A
• gnomAD v3: 9-37442184-G-A
• gnomAD v4: 9-37442184-G-A
• MyVariant Identifiers: chr9:g.37442181G>A (hg19) ; chr9:g.37442184G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37442184G>A , CM000671.2:g.37442184G>A	GRCh38
NC_000009.11:g.37442181G>A , CM000671.1:g.37442181G>A	GRCh37
NC_000009.10:g.37432181G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307750.5:c.368C>T MANE Select	ENSP00000307604.4:p.Thr123Met
ENST00000307750.4:c.368C>T	ENSP00000307604.4:p.Thr123Met
NM_014872.2:c.368C>T	NP_055687.1:p.Thr123Met
XM_005251634.1:c.368C>T	XP_005251691.1:p.Thr123Met
XM_005251634.2:c.368C>T	XP_005251691.1:p.Thr123Met
NM_014872.3:c.368C>T MANE Select	NP_055687.1:p.Thr123Met