Canonical Allele Identifier: CA1180535144
Gene: TGFBR3 HGNC NCBI

Linked Data

dbSNP Id: rs1678408033

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.91866849G>C , CM000663.2:g.91866849G>C GRCh38
NC_000001.10:g.92332406G>C , CM000663.1:g.92332406G>C GRCh37
NC_000001.9:g.92104994G>C NCBI36
NG_027757.1:g.44154C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000212355.9:c.-113-5205C>G MANE Select ENSP00000212355.4:n.-113-5205C>G
ENST00000212355.8:c.-113-5205C>G ENSP00000212355.4:n.-113-5205C>G
ENST00000370399.6:c.-113-5205C>G ENSP00000359426.2:n.-113-5205C>G
ENST00000417833.2:c.-200-7C>G ENSP00000395975.2:n.-200-7C>G
ENST00000465892.6:c.-113-5205C>G ENSP00000432638.1:n.-113-5205C>G
ENST00000532540.5:c.-113-5205C>G ENSP00000434994.1:n.-113-5205C>G
ENST00000533370.1:n.123-2570C>G
NM_001195683.1:c.-113-5205C>G NP_001182612.1:n.-113-5205C>G
NM_001195684.1:c.-113-5205C>G NP_001182613.1:n.-113-5205C>G
NM_003243.4:c.-113-5205C>G NP_003234.2:n.-113-5205C>G
NR_036634.1:n.403-5205C>G
XM_006710867.1:c.-113-5205C>G XP_006710930.1:n.-113-5205C>G
XM_006710867.2:c.-113-5205C>G XP_006710930.1:n.-113-5205C>G
NM_003243.5:c.-113-5205C>G MANE Select NP_003234.2:n.-113-5205C>G
NM_001195683.2:c.-113-5205C>G NP_001182612.1:n.-113-5205C>G
NR_036634.2:n.275-5205C>G