Canonical Allele Identifier: CA2744558641
Gene: TGFBR3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.91866940A>G , CM000663.2:g.91866940A>G GRCh38
NC_000001.10:g.92332497A>G , CM000663.1:g.92332497A>G GRCh37
NC_000001.9:g.92105085A>G NCBI36
NG_027757.1:g.44063T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000212355.9:c.-113-5296T>C MANE Select ENSP00000212355.4:n.-113-5296T>C
ENST00000212355.8:c.-113-5296T>C ENSP00000212355.4:n.-113-5296T>C
ENST00000370399.6:c.-113-5296T>C ENSP00000359426.2:n.-113-5296T>C
ENST00000417833.2:c.-200-98T>C ENSP00000395975.2:n.-200-98T>C
ENST00000465892.6:c.-113-5296T>C ENSP00000432638.1:n.-113-5296T>C
ENST00000532540.5:c.-113-5296T>C ENSP00000434994.1:n.-113-5296T>C
ENST00000533370.1:n.123-2661T>C
NM_001195683.1:c.-113-5296T>C NP_001182612.1:n.-113-5296T>C
NM_001195684.1:c.-113-5296T>C NP_001182613.1:n.-113-5296T>C
NM_003243.4:c.-113-5296T>C NP_003234.2:n.-113-5296T>C
NR_036634.1:n.403-5296T>C
XM_006710867.1:c.-113-5296T>C XP_006710930.1:n.-113-5296T>C
XM_006710867.2:c.-113-5296T>C XP_006710930.1:n.-113-5296T>C
NM_003243.5:c.-113-5296T>C MANE Select NP_003234.2:n.-113-5296T>C
NM_001195683.2:c.-113-5296T>C NP_001182612.1:n.-113-5296T>C
NR_036634.2:n.275-5296T>C