Canonical Allele Identifier: CA344725379
Gene: TGFB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.218346842G>T , CM000663.2:g.218346842G>T GRCh38
NC_000001.10:g.218520184G>T , CM000663.1:g.218520184G>T GRCh37
NC_000001.9:g.216586807G>T NCBI36
NG_027721.1:g.6509G>T
NG_027721.2:g.6509G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000366930.9:c.141G>T MANE Select ENSP00000355897.4:p.Lys47Asn
ENST00000366929.4:c.141G>T ENSP00000355896.4:p.Lys47Asn
ENST00000366930.8:c.141G>T ENSP00000355897.4:p.Lys47Asn
NM_001135599.2:c.141G>T NP_001129071.1:p.Lys47Asn
NM_003238.3:c.141G>T NP_003229.1:p.Lys47Asn
NM_001135599.3:c.141G>T NP_001129071.1:p.Lys47Asn
NM_003238.4:c.141G>T NP_003229.1:p.Lys47Asn
NR_138148.1:n.1559G>T
NR_138149.1:n.1559G>T
NM_003238.5:c.141G>T NP_003229.1:p.Lys47Asn
NM_003238.6:c.141G>T MANE Select NP_003229.1:p.Lys47Asn
NM_001135599.4:c.141G>T NP_001129071.1:p.Lys47Asn
NR_138148.2:n.1507G>T
NR_138149.2:n.1507G>T