Canonical Allele Identifier: CA2480603246
Gene: GATAD2B HGNC NCBI

Linked Data

dbSNP Id: rs757864430

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153819754A>C , CM000663.2:g.153819754A>C GRCh38
NC_000001.10:g.153792230A>C , CM000663.1:g.153792230A>C GRCh37
NC_000001.9:g.152058854A>C NCBI36
NG_050988.1:g.108222T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000703630.1:c.-88-19T>G ENSP00000515408.1:n.-88-19T>G
ENST00000368655.5:c.336-19T>G MANE Select ENSP00000357644.4:n.336-19T>G
ENST00000638051.1:n.54-19T>G
ENST00000368655.4:c.336-19T>G ENSP00000357644.4:n.336-19T>G
ENST00000634401.1:c.336-19T>G ENSP00000489313.1:n.336-19T>G
ENST00000634408.1:c.336-19T>G ENSP00000489595.1:n.336-19T>G
ENST00000634544.1:c.336-19T>G ENSP00000489184.1:n.336-19T>G
ENST00000634791.1:c.336-19T>G ENSP00000489566.1:n.336-19T>G
NM_020699.2:c.336-19T>G NP_065750.1:n.336-19T>G
XM_005245364.3:c.336-19T>G XP_005245421.1:n.336-19T>G
XM_006711469.2:c.336-19T>G XP_006711532.1:n.336-19T>G
XM_011509808.1:c.336-19T>G XP_011508110.1:n.336-19T>G
NM_020699.3:c.336-19T>G NP_065750.1:n.336-19T>G
XM_005245364.4:c.336-19T>G XP_005245421.1:n.336-19T>G
XM_024448621.1:c.336-19T>G XP_024304389.1:n.336-19T>G
NM_020699.4:c.336-19T>G MANE Select NP_065750.1:n.336-19T>G