Canonical Allele Identifier: CA646427569

Gene: TGFB2

Linked Data

• dbSNP Id: rs1660150701
• gnomAD v4: 1-218441483-A-T
• COSMIC: COSN7985395

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218441483A>T , CM000663.2:g.218441483A>T	GRCh38
NC_000001.10:g.218614825A>T , CM000663.1:g.218614825A>T	GRCh37
NC_000001.9:g.216681448A>T	NCBI36
NG_027721.1:g.101150A>T
NG_027721.2:g.101150A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.*121A>T MANE Select	ENSP00000355897.4:n.*121A>T
ENST00000366929.4:c.*121A>T	ENSP00000355896.4:n.*121A>T
ENST00000366930.8:c.*121A>T	ENSP00000355897.4:n.*121A>T
ENST00000479322.1:n.850A>T
NM_001135599.2:c.*121A>T	NP_001129071.1:n.*121A>T
NM_003238.3:c.*121A>T	NP_003229.1:n.*121A>T
NM_001135599.3:c.*121A>T	NP_001129071.1:n.*121A>T
NM_003238.4:c.*121A>T	NP_003229.1:n.*121A>T
NR_138148.1:n.2669A>T
NR_138149.1:n.2753A>T
NM_003238.5:c.*121A>T	NP_003229.1:n.*121A>T
NM_003238.6:c.*121A>T MANE Select	NP_003229.1:n.*121A>T
NM_001135599.4:c.*121A>T	NP_001129071.1:n.*121A>T
NR_138148.2:n.2617A>T
NR_138149.2:n.2701A>T