Canonical Allele Identifier: CA420946149

Gene: GATAD2B

Linked Data

• MyVariant Identifiers: chr1:g.153788927G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153816451G>T , CM000663.2:g.153816451G>T	GRCh38
NC_000001.10:g.153788927G>T , CM000663.1:g.153788927G>T	GRCh37
NC_000001.9:g.152055551G>T	NCBI36
NG_050988.1:g.111525C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000703630.1:c.615C>A	ENSP00000515408.1:p.Ala205=
ENST00000368655.5:c.1038C>A MANE Select	ENSP00000357644.4:p.Ala346=
ENST00000368655.4:c.1038C>A	ENSP00000357644.4:p.Ala346=
ENST00000634408.1:c.990C>A	ENSP00000489595.1:p.Ala330=
ENST00000634544.1:c.1038C>A	ENSP00000489184.1:p.Ala346=
ENST00000634564.1:c.292C>A
NM_020699.2:c.1038C>A	NP_065750.1:p.Ala346=
XM_005245364.3:c.1038C>A	XP_005245421.1:p.Ala346=
XM_006711469.2:c.1038C>A	XP_006711532.1:p.Ala346=
XM_011509808.1:c.1038C>A	XP_011508110.1:p.Ala346=
NM_020699.3:c.1038C>A	NP_065750.1:p.Ala346=
XM_005245364.4:c.1038C>A	XP_005245421.1:p.Ala346=
XM_024448621.1:c.1038C>A	XP_024304389.1:p.Ala346=
NM_020699.4:c.1038C>A MANE Select	NP_065750.1:p.Ala346=