Canonical Allele Identifier: CA2650531403

Gene: TGFB2

Linked Data

• gnomAD v4: 1-218434277-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218434277A>T , CM000663.2:g.218434277A>T	GRCh38
NC_000001.10:g.218607619A>T , CM000663.1:g.218607619A>T	GRCh37
NC_000001.9:g.216674242A>T	NCBI36
NG_027721.1:g.93944A>T
NG_027721.2:g.93944A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000366930.9:c.644-61A>T MANE Select	ENSP00000355897.4:n.644-61A>T
ENST00000366929.4:c.728-61A>T	ENSP00000355896.4:n.728-61A>T
ENST00000366930.8:c.644-61A>T	ENSP00000355897.4:n.644-61A>T
ENST00000479322.1:n.127+25A>T
ENST00000488793.1:n.370A>T
NM_001135599.2:c.728-61A>T	NP_001129071.1:n.728-61A>T
NM_003238.3:c.644-61A>T	NP_003229.1:n.644-61A>T
NM_001135599.3:c.728-61A>T	NP_001129071.1:n.728-61A>T
NM_003238.4:c.644-61A>T	NP_003229.1:n.644-61A>T
NR_138148.1:n.2062-61A>T
NR_138149.1:n.2146-61A>T
NM_003238.5:c.644-61A>T	NP_003229.1:n.644-61A>T
NM_003238.6:c.644-61A>T MANE Select	NP_003229.1:n.644-61A>T
NM_001135599.4:c.728-61A>T	NP_001129071.1:n.728-61A>T
NR_138148.2:n.2010-61A>T
NR_138149.2:n.2094-61A>T