Canonical Allele Identifier: CA342527592

Gene: GATAD2B

Linked Data

• MyVariant Identifiers: chr1:g.153788926T>C (hg19) ; chr1:g.153816450T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153816450T>C , CM000663.2:g.153816450T>C	GRCh38
NC_000001.10:g.153788926T>C , CM000663.1:g.153788926T>C	GRCh37
NC_000001.9:g.152055550T>C	NCBI36
NG_050988.1:g.111526A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000703630.1:c.616A>G	ENSP00000515408.1:p.Asn206Asp
ENST00000368655.5:c.1039A>G MANE Select	ENSP00000357644.4:p.Asn347Asp
ENST00000368655.4:c.1039A>G	ENSP00000357644.4:p.Asn347Asp
ENST00000634408.1:c.991A>G	ENSP00000489595.1:p.Asn331Asp
ENST00000634544.1:c.1039A>G	ENSP00000489184.1:p.Asn347Asp
ENST00000634564.1:c.293A>G
NM_020699.2:c.1039A>G	NP_065750.1:p.Asn347Asp
XM_005245364.3:c.1039A>G	XP_005245421.1:p.Asn347Asp
XM_006711469.2:c.1039A>G	XP_006711532.1:p.Asn347Asp
XM_011509808.1:c.1039A>G	XP_011508110.1:p.Asn347Asp
NM_020699.3:c.1039A>G	NP_065750.1:p.Asn347Asp
XM_005245364.4:c.1039A>G	XP_005245421.1:p.Asn347Asp
XM_024448621.1:c.1039A>G	XP_024304389.1:p.Asn347Asp
NM_020699.4:c.1039A>G MANE Select	NP_065750.1:p.Asn347Asp