Canonical Allele Identifier: CA2839265399
Gene: TGFBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30691358C>T , CM000665.2:g.30691358C>T GRCh38
NC_000003.11:g.30732850C>T , CM000665.1:g.30732850C>T GRCh37
NC_000003.10:g.30707854C>T NCBI36
NG_007490.1:g.89857C>T , LRG_779:g.89857C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.1525-62C>T MANE Select ENSP00000295754.5:n.1525-62C>T
ENST00000672050.1:n.409-62C>T
ENST00000672866.1:n.3121-62C>T
ENST00000673203.1:n.403-62C>T
ENST00000295754.9:c.1525-62C>T ENSP00000295754.5:n.1525-62C>T
ENST00000359013.4:c.1600-62C>T ENSP00000351905.4:n.1600-62C>T
NM_001024847.2:c.1600-62C>T , LRG_779t1:c.1600-62C>T NP_001020018.1:n.1600-62C>T
NM_003242.5:c.1525-62C>T NP_003233.4:n.1525-62C>T
XM_011534043.1:c.1552-62C>T XP_011532345.1:n.1552-62C>T
XM_011534044.1:c.1477-62C>T XP_011532346.1:n.1477-62C>T
XM_011534045.1:c.1420-62C>T XP_011532347.1:n.1420-62C>T
XM_011534043.2:c.1552-62C>T XP_011532345.1:n.1552-62C>T
XM_011534045.3:c.1420-62C>T XP_011532347.1:n.1420-62C>T
XM_017007106.1:c.1420-62C>T XP_016862595.1:n.1420-62C>T
NM_003242.6:c.1525-62C>T MANE Select NP_003233.4:n.1525-62C>T