Canonical Allele Identifier: CA342523700

Gene: GATAD2B

Linked Data

• MyVariant Identifiers: chr1:g.153785735C>G (hg19) ; chr1:g.153813259C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153813259C>G , CM000663.2:g.153813259C>G	GRCh38
NC_000001.10:g.153785735C>G , CM000663.1:g.153785735C>G	GRCh37
NC_000001.9:g.152052359C>G	NCBI36
NG_050988.1:g.114717G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000368655.5:c.1410G>C MANE Select	ENSP00000357644.4:p.Gln470His
ENST00000368655.4:c.1410G>C	ENSP00000357644.4:p.Gln470His
ENST00000634408.1:c.1362G>C	ENSP00000489595.1:p.Gln454His
ENST00000634544.1:c.1410G>C	ENSP00000489184.1:p.Gln470His
ENST00000634564.1:c.664G>C
NM_020699.2:c.1410G>C	NP_065750.1:p.Gln470His
XM_005245364.3:c.1410G>C	XP_005245421.1:p.Gln470His
XM_006711469.2:c.1410G>C	XP_006711532.1:p.Gln470His
XM_011509808.1:c.1410G>C	XP_011508110.1:p.Gln470His
NM_020699.3:c.1410G>C	NP_065750.1:p.Gln470His
XM_005245364.4:c.1410G>C	XP_005245421.1:p.Gln470His
XM_024448621.1:c.1410G>C	XP_024304389.1:p.Gln470His
NM_020699.4:c.1410G>C MANE Select	NP_065750.1:p.Gln470His