Canonical Allele Identifier: CA342535318
Gene: GATAD2B HGNC NCBI

Linked Data

dbSNP Id: rs1427914859

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153819665G>C , CM000663.2:g.153819665G>C GRCh38
NC_000001.10:g.153792141G>C , CM000663.1:g.153792141G>C GRCh37
NC_000001.9:g.152058765G>C NCBI36
NG_050988.1:g.108311C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000703630.1:c.-18C>G ENSP00000515408.1:n.-18C>G
ENST00000368655.5:c.406C>G MANE Select ENSP00000357644.4:p.Pro136Ala
ENST00000368655.4:c.406C>G ENSP00000357644.4:p.Pro136Ala
ENST00000634401.1:c.406C>G ENSP00000489313.1:p.Pro136Ala
ENST00000634408.1:c.406C>G ENSP00000489595.1:p.Pro136Ala
ENST00000634544.1:c.406C>G ENSP00000489184.1:p.Pro136Ala
ENST00000634791.1:c.406C>G ENSP00000489566.1:p.Pro136Ala
NM_020699.2:c.406C>G NP_065750.1:p.Pro136Ala
XM_005245364.3:c.406C>G XP_005245421.1:p.Pro136Ala
XM_006711469.2:c.406C>G XP_006711532.1:p.Pro136Ala
XM_011509808.1:c.406C>G XP_011508110.1:p.Pro136Ala
NM_020699.3:c.406C>G NP_065750.1:p.Pro136Ala
XM_005245364.4:c.406C>G XP_005245421.1:p.Pro136Ala
XM_024448621.1:c.406C>G XP_024304389.1:p.Pro136Ala
NM_020699.4:c.406C>G MANE Select NP_065750.1:p.Pro136Ala