Canonical Allele Identifier: CA342524362

Gene: GATAD2B

Linked Data

• MyVariant Identifiers: chr1:g.153785815A>T (hg19) ; chr1:g.153813339A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153813339A>T , CM000663.2:g.153813339A>T	GRCh38
NC_000001.10:g.153785815A>T , CM000663.1:g.153785815A>T	GRCh37
NC_000001.9:g.152052439A>T	NCBI36
NG_050988.1:g.114637T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000368655.5:c.1330T>A MANE Select	ENSP00000357644.4:p.Cys444Ser
ENST00000368655.4:c.1330T>A	ENSP00000357644.4:p.Cys444Ser
ENST00000634408.1:c.1282T>A	ENSP00000489595.1:p.Cys428Ser
ENST00000634544.1:c.1330T>A	ENSP00000489184.1:p.Cys444Ser
ENST00000634564.1:c.584T>A
NM_020699.2:c.1330T>A	NP_065750.1:p.Cys444Ser
XM_005245364.3:c.1330T>A	XP_005245421.1:p.Cys444Ser
XM_006711469.2:c.1330T>A	XP_006711532.1:p.Cys444Ser
XM_011509808.1:c.1330T>A	XP_011508110.1:p.Cys444Ser
NM_020699.3:c.1330T>A	NP_065750.1:p.Cys444Ser
XM_005245364.4:c.1330T>A	XP_005245421.1:p.Cys444Ser
XM_024448621.1:c.1330T>A	XP_024304389.1:p.Cys444Ser
NM_020699.4:c.1330T>A MANE Select	NP_065750.1:p.Cys444Ser