Canonical Allele Identifier: CA1354873957
Gene: TGFBR2 HGNC NCBI

Linked Data

dbSNP Id: rs1699388607
gnomAD v4: 3-30674051-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30674051A>C , CM000665.2:g.30674051A>C GRCh38
NC_000003.11:g.30715543A>C , CM000665.1:g.30715543A>C GRCh37
NC_000003.10:g.30690547A>C NCBI36
NG_007490.1:g.72550A>C , LRG_779:g.72550A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000295754.10:c.1255-54A>C MANE Select ENSP00000295754.5:n.1255-54A>C
ENST00000672866.1:n.2851-54A>C
ENST00000673203.1:n.79A>C
ENST00000295754.9:c.1255-54A>C ENSP00000295754.5:n.1255-54A>C
ENST00000359013.4:c.1330-54A>C ENSP00000351905.4:n.1330-54A>C
NM_001024847.2:c.1330-54A>C , LRG_779t1:c.1330-54A>C NP_001020018.1:n.1330-54A>C
NM_003242.5:c.1255-54A>C NP_003233.4:n.1255-54A>C
XM_011534043.1:c.1282-54A>C XP_011532345.1:n.1282-54A>C
XM_011534044.1:c.1207-54A>C XP_011532346.1:n.1207-54A>C
XM_011534045.1:c.1150-54A>C XP_011532347.1:n.1150-54A>C
XM_011534043.2:c.1282-54A>C XP_011532345.1:n.1282-54A>C
XM_011534045.3:c.1150-54A>C XP_011532347.1:n.1150-54A>C
XM_017007106.1:c.1150-54A>C XP_016862595.1:n.1150-54A>C
NM_003242.6:c.1255-54A>C MANE Select NP_003233.4:n.1255-54A>C