Canonical Allele Identifier: CA433059086
Gene: TGFBR2 HGNC NCBI

Linked Data

dbSNP Id: rs1436199311
MyVariant Identifiers: chr3:g.30713743G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30672251G>T , CM000665.2:g.30672251G>T GRCh38
NC_000003.11:g.30713743G>T , CM000665.1:g.30713743G>T GRCh37
NC_000003.10:g.30688747G>T NCBI36
NG_007490.1:g.70750G>T , LRG_779:g.70750G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000295754.10:c.1068G>T MANE Select ENSP00000295754.5:p.Arg356=
ENST00000672866.1:n.2664G>T
ENST00000295754.9:c.1068G>T ENSP00000295754.5:p.Arg356=
ENST00000359013.4:c.1143G>T ENSP00000351905.4:p.Arg381=
NM_001024847.2:c.1143G>T , LRG_779t1:c.1143G>T NP_001020018.1:p.Arg381=
NM_003242.5:c.1068G>T NP_003233.4:p.Arg356=
XM_011534043.1:c.1095G>T XP_011532345.1:p.Arg365=
XM_011534044.1:c.1020G>T XP_011532346.1:p.Arg340=
XM_011534045.1:c.963G>T XP_011532347.1:p.Arg321=
XM_011534043.2:c.1095G>T XP_011532345.1:p.Arg365=
XM_011534045.3:c.963G>T XP_011532347.1:p.Arg321=
XM_017007106.1:c.963G>T XP_016862595.1:p.Arg321=
NM_003242.6:c.1068G>T MANE Select NP_003233.4:p.Arg356=