Canonical Allele Identifier: CA1221568492

Gene: TGFB2

Linked Data

• dbSNP Id: rs1660151294
• gnomAD v4: 1-218441499-TACTAGTTCAGAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218441503_218441514del , CM000663.2:g.218441503_218441514del	GRCh38
NC_000001.10:g.218614845_218614856del , CM000663.1:g.218614845_218614856del	GRCh37
NC_000001.9:g.216681468_216681479del	NCBI36
NG_027721.1:g.101170_101181del
NG_027721.2:g.101170_101181del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.*141_*152del MANE Select	ENSP00000355897.4:n.*141_*152del
ENST00000366929.4:c.*141_*152del	ENSP00000355896.4:n.*141_*152del
ENST00000366930.8:c.*141_*152del	ENSP00000355897.4:n.*141_*152del
ENST00000479322.1:n.870_881del
NM_001135599.2:c.*141_*152del	NP_001129071.1:n.*141_*152del
NM_003238.3:c.*141_*152del	NP_003229.1:n.*141_*152del
NM_001135599.3:c.*141_*152del	NP_001129071.1:n.*141_*152del
NM_003238.4:c.*141_*152del	NP_003229.1:n.*141_*152del
NR_138148.1:n.2689_2700del
NR_138149.1:n.2773_2784del
NM_003238.5:c.*141_*152del	NP_003229.1:n.*141_*152del
NM_003238.6:c.*141_*152del MANE Select	NP_003229.1:n.*141_*152del
NM_001135599.4:c.*141_*152del	NP_001129071.1:n.*141_*152del
NR_138148.2:n.2637_2648del
NR_138149.2:n.2721_2732del