Canonical Allele Identifier: CA344727767

Gene: TGFB2

Linked Data

• MyVariant Identifiers: chr1:g.218614553G>A (hg19) ; chr1:g.218441211G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218441211G>A , CM000663.2:g.218441211G>A	GRCh38
NC_000001.10:g.218614553G>A , CM000663.1:g.218614553G>A	GRCh37
NC_000001.9:g.216681176G>A	NCBI36
NG_027721.1:g.100878G>A
NG_027721.2:g.100878G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.1094G>A MANE Select	ENSP00000355897.4:p.Ser365Asn
ENST00000366929.4:c.1178G>A	ENSP00000355896.4:p.Ser393Asn
ENST00000366930.8:c.1094G>A	ENSP00000355897.4:p.Ser365Asn
ENST00000479322.1:n.578G>A
NM_001135599.2:c.1178G>A	NP_001129071.1:p.Ser393Asn
NM_003238.3:c.1094G>A	NP_003229.1:p.Ser365Asn
NM_001135599.3:c.1178G>A	NP_001129071.1:p.Ser393Asn
NM_003238.4:c.1094G>A	NP_003229.1:p.Ser365Asn
NR_138148.1:n.2397G>A
NR_138149.1:n.2481G>A
NM_003238.5:c.1094G>A	NP_003229.1:p.Ser365Asn
NM_003238.6:c.1094G>A MANE Select	NP_003229.1:p.Ser365Asn
NM_001135599.4:c.1178G>A	NP_001129071.1:p.Ser393Asn
NR_138148.2:n.2345G>A
NR_138149.2:n.2429G>A