Canonical Allele Identifier: CA10687414

Gene: GATAD2B

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153876520G>A , CM000663.2:g.153876520G>A	GRCh38
NC_000001.10:g.153848996G>A , CM000663.1:g.153848996G>A	GRCh37
NC_000001.9:g.152115620G>A	NCBI36
NG_050988.1:g.51456C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703630.1:c.-89+46213C>T	ENSP00000515408.1:n.-89+46213C>T
ENST00000368655.5:c.-2+46213C>T MANE Select	ENSP00000357644.4:n.-2+46213C>T
ENST00000636014.1:n.96+22336C>T
ENST00000637331.1:c.-2+46779C>T	ENSP00000490635.1:n.-2+46779C>T
ENST00000368655.4:c.-2+46213C>T	ENSP00000357644.4:n.-2+46213C>T
ENST00000634401.1:c.-2+38154C>T	ENSP00000489313.1:n.-2+38154C>T
ENST00000634408.1:c.-2+46213C>T	ENSP00000489595.1:n.-2+46213C>T
ENST00000634544.1:c.-2+45319C>T	ENSP00000489184.1:n.-2+45319C>T
ENST00000634791.1:c.-2+9904C>T	ENSP00000489566.1:n.-2+9904C>T
NM_020699.2:c.-2+46213C>T	NP_065750.1:n.-2+46213C>T
XM_005245364.3:c.-2+16786C>T	XP_005245421.1:n.-2+16786C>T
XM_011509808.1:c.-2+22336C>T	XP_011508110.1:n.-2+22336C>T
NM_020699.3:c.-2+46213C>T	NP_065750.1:n.-2+46213C>T
XM_005245364.4:c.-2+16786C>T	XP_005245421.1:n.-2+16786C>T
XM_024448621.1:c.-2+46779C>T	XP_024304389.1:n.-2+46779C>T
NM_020699.4:c.-2+46213C>T MANE Select	NP_065750.1:n.-2+46213C>T