Canonical Allele Identifier: CA1046445453
Gene: TGFBR2 HGNC NCBI

Linked Data

gnomAD v3: 3-30668595-G-T
gnomAD v4: 3-30668595-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30668595G>T , CM000665.2:g.30668595G>T GRCh38
NC_000003.11:g.30710087G>T , CM000665.1:g.30710087G>T GRCh37
NC_000003.10:g.30685091G>T NCBI36
NG_007490.1:g.67094G>T , LRG_779:g.67094G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.455-3043G>T MANE Select ENSP00000295754.5:n.455-3043G>T
ENST00000672866.1:n.2051-3043G>T
ENST00000295754.9:c.455-3043G>T ENSP00000295754.5:n.455-3043G>T
ENST00000359013.4:c.530-3043G>T ENSP00000351905.4:n.530-3043G>T
NM_001024847.2:c.530-3043G>T , LRG_779t1:c.530-3043G>T NP_001020018.1:n.530-3043G>T
NM_003242.5:c.455-3043G>T NP_003233.4:n.455-3043G>T
XM_011534043.1:c.482-3043G>T XP_011532345.1:n.482-3043G>T
XM_011534044.1:c.407-3043G>T XP_011532346.1:n.407-3043G>T
XM_011534045.1:c.350-3043G>T XP_011532347.1:n.350-3043G>T
XM_011534043.2:c.482-3043G>T XP_011532345.1:n.482-3043G>T
XM_011534045.3:c.350-3043G>T XP_011532347.1:n.350-3043G>T
XM_017007106.1:c.350-3043G>T XP_016862595.1:n.350-3043G>T
NM_003242.6:c.455-3043G>T MANE Select NP_003233.4:n.455-3043G>T