Canonical Allele Identifier: CA2650532798

Gene: TGFB2

Linked Data

• gnomAD v4: 1-218441601-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218441601G>T , CM000663.2:g.218441601G>T	GRCh38
NC_000001.10:g.218614943G>T , CM000663.1:g.218614943G>T	GRCh37
NC_000001.9:g.216681566G>T	NCBI36
NG_027721.1:g.101268G>T
NG_027721.2:g.101268G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.*239G>T MANE Select	ENSP00000355897.4:n.*239G>T
ENST00000366929.4:c.*239G>T	ENSP00000355896.4:n.*239G>T
ENST00000366930.8:c.*239G>T	ENSP00000355897.4:n.*239G>T
ENST00000479322.1:n.968G>T
NM_001135599.2:c.*239G>T	NP_001129071.1:n.*239G>T
NM_003238.3:c.*239G>T	NP_003229.1:n.*239G>T
NM_001135599.3:c.*239G>T	NP_001129071.1:n.*239G>T
NM_003238.4:c.*239G>T	NP_003229.1:n.*239G>T
NR_138148.1:n.2787G>T
NR_138149.1:n.2871G>T
NM_003238.5:c.*239G>T	NP_003229.1:n.*239G>T
NM_003238.6:c.*239G>T MANE Select	NP_003229.1:n.*239G>T
NM_001135599.4:c.*239G>T	NP_001129071.1:n.*239G>T
NR_138148.2:n.2735G>T
NR_138149.2:n.2819G>T