Canonical Allele Identifier: CA342527599

Gene: GATAD2B

Linked Data

• MyVariant Identifiers: chr1:g.153788928G>A (hg19) ; chr1:g.153816452G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153816452G>A , CM000663.2:g.153816452G>A	GRCh38
NC_000001.10:g.153788928G>A , CM000663.1:g.153788928G>A	GRCh37
NC_000001.9:g.152055552G>A	NCBI36
NG_050988.1:g.111524C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000703630.1:c.614C>T	ENSP00000515408.1:p.Ala205Val
ENST00000368655.5:c.1037C>T MANE Select	ENSP00000357644.4:p.Ala346Val
ENST00000368655.4:c.1037C>T	ENSP00000357644.4:p.Ala346Val
ENST00000634408.1:c.989C>T	ENSP00000489595.1:p.Ala330Val
ENST00000634544.1:c.1037C>T	ENSP00000489184.1:p.Ala346Val
ENST00000634564.1:c.291C>T
NM_020699.2:c.1037C>T	NP_065750.1:p.Ala346Val
XM_005245364.3:c.1037C>T	XP_005245421.1:p.Ala346Val
XM_006711469.2:c.1037C>T	XP_006711532.1:p.Ala346Val
XM_011509808.1:c.1037C>T	XP_011508110.1:p.Ala346Val
NM_020699.3:c.1037C>T	NP_065750.1:p.Ala346Val
XM_005245364.4:c.1037C>T	XP_005245421.1:p.Ala346Val
XM_024448621.1:c.1037C>T	XP_024304389.1:p.Ala346Val
NM_020699.4:c.1037C>T MANE Select	NP_065750.1:p.Ala346Val