Canonical Allele Identifier: CA344727874

Gene: TGFB2

Linked Data

• MyVariant Identifiers: chr1:g.218614601T>C (hg19) ; chr1:g.218441259T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218441259T>C , CM000663.2:g.218441259T>C	GRCh38
NC_000001.10:g.218614601T>C , CM000663.1:g.218614601T>C	GRCh37
NC_000001.9:g.216681224T>C	NCBI36
NG_027721.1:g.100926T>C
NG_027721.2:g.100926T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.1142T>C MANE Select	ENSP00000355897.4:p.Val381Ala
ENST00000366929.4:c.1226T>C	ENSP00000355896.4:p.Val409Ala
ENST00000366930.8:c.1142T>C	ENSP00000355897.4:p.Val381Ala
ENST00000479322.1:n.626T>C
NM_001135599.2:c.1226T>C	NP_001129071.1:p.Val409Ala
NM_003238.3:c.1142T>C	NP_003229.1:p.Val381Ala
NM_001135599.3:c.1226T>C	NP_001129071.1:p.Val409Ala
NM_003238.4:c.1142T>C	NP_003229.1:p.Val381Ala
NR_138148.1:n.2445T>C
NR_138149.1:n.2529T>C
NM_003238.5:c.1142T>C	NP_003229.1:p.Val381Ala
NM_003238.6:c.1142T>C MANE Select	NP_003229.1:p.Val381Ala
NM_001135599.4:c.1226T>C	NP_001129071.1:p.Val409Ala
NR_138148.2:n.2393T>C
NR_138149.2:n.2477T>C