Canonical Allele Identifier: CA045424
Gene: TGFBR2 HGNC NCBI

Linked Data

dbSNP Id: rs750658746
gnomAD v2: 3-30713699-A-T
gnomAD v4: 3-30672207-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30672207A>T , CM000665.2:g.30672207A>T GRCh38
NC_000003.11:g.30713699A>T , CM000665.1:g.30713699A>T GRCh37
NC_000003.10:g.30688703A>T NCBI36
NG_007490.1:g.70706A>T , LRG_779:g.70706A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.1024A>T MANE Select ENSP00000295754.5:p.Ile342Phe
ENST00000672866.1:n.2620A>T
ENST00000295754.9:c.1024A>T ENSP00000295754.5:p.Ile342Phe
ENST00000359013.4:c.1099A>T ENSP00000351905.4:p.Ile367Phe
NM_001024847.2:c.1099A>T , LRG_779t1:c.1099A>T NP_001020018.1:p.Ile367Phe
NM_003242.5:c.1024A>T NP_003233.4:p.Ile342Phe
XM_011534043.1:c.1051A>T XP_011532345.1:p.Ile351Phe
XM_011534044.1:c.976A>T XP_011532346.1:p.Ile326Phe
XM_011534045.1:c.919A>T XP_011532347.1:p.Ile307Phe
XM_011534043.2:c.1051A>T XP_011532345.1:p.Ile351Phe
XM_011534045.3:c.919A>T XP_011532347.1:p.Ile307Phe
XM_017007106.1:c.919A>T XP_016862595.1:p.Ile307Phe
NM_003242.6:c.1024A>T MANE Select NP_003233.4:p.Ile342Phe