Canonical Allele Identifier: CA344727606

Gene: TGFB2

Linked Data

• MyVariant Identifiers: chr1:g.218610782A>C (hg19) ; chr1:g.218437440A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218437440A>C , CM000663.2:g.218437440A>C	GRCh38
NC_000001.10:g.218610782A>C , CM000663.1:g.218610782A>C	GRCh37
NC_000001.9:g.216677405A>C	NCBI36
NG_027721.1:g.97107A>C
NG_027721.2:g.97107A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000366930.9:c.1030A>C MANE Select	ENSP00000355897.4:p.Asn344His
ENST00000366929.4:c.1114A>C	ENSP00000355896.4:p.Asn372His
ENST00000366930.8:c.1030A>C	ENSP00000355897.4:p.Asn344His
ENST00000479322.1:n.514A>C
NM_001135599.2:c.1114A>C	NP_001129071.1:p.Asn372His
NM_003238.3:c.1030A>C	NP_003229.1:p.Asn344His
NM_001135599.3:c.1114A>C	NP_001129071.1:p.Asn372His
NM_003238.4:c.1030A>C	NP_003229.1:p.Asn344His
NR_138148.1:n.2333A>C
NR_138149.1:n.2417A>C
NM_003238.5:c.1030A>C	NP_003229.1:p.Asn344His
NM_003238.6:c.1030A>C MANE Select	NP_003229.1:p.Asn344His
NM_001135599.4:c.1114A>C	NP_001129071.1:p.Asn372His
NR_138148.2:n.2281A>C
NR_138149.2:n.2365A>C