Canonical Allele Identifier: CA10680101
Gene: TGFBR3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2489188

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.91866932C>T , CM000663.2:g.91866932C>T GRCh38
NC_000001.9:g.92105077C>T NCBI36
NC_000001.10:g.92332489C>T , CM000663.1:g.92332489C>T GRCh37
NG_027757.1:g.44071G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000212355.8:c.-113-5288G>A ENSP00000212355.4:p.=
ENST00000370399.6:c.-113-5288G>A ENSP00000359426.2:p.=
ENST00000417833.2:c.-200-90G>A ENSP00000395975.2:p.=
ENST00000465892.6:c.-113-5288G>A ENSP00000432638.1:p.=
ENST00000532540.5:c.-113-5288G>A ENSP00000434994.1:p.=
ENST00000533370.1:n.123-2653G>A
NM_001195683.1:c.-113-5288G>A VV NP_001182612.1:p.=
NM_001195684.1:c.-113-5288G>A VV NP_001182613.1:p.=
NM_003243.4:c.-113-5288G>A VV NP_003234.2:p.=
NR_036634.1:n.403-5288G>A
XM_006710867.1:c.-113-5288G>A XP_006710930.1:p.=