Canonical Allele Identifier: CA2664866611
Gene: TGFBR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30606773_30606774insAC , CM000665.2:g.30606773_30606774insAC GRCh38
NC_000003.11:g.30648265_30648266insAC , CM000665.1:g.30648265_30648266insAC GRCh37
NC_000003.10:g.30623269_30623270insAC NCBI36
NG_007490.1:g.5272_5273insAC , LRG_779:g.5272_5273insAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.-111_-110insAC MANE Select ENSP00000295754.5:n.-111_-110insAC
ENST00000295754.9:c.-111_-110insAC ENSP00000295754.5:n.-111_-110insAC
ENST00000359013.4:c.-111_-110insAC ENSP00000351905.4:n.-111_-110insAC
NM_001024847.2:c.-111_-110insAC , LRG_779t1:c.-111_-110insAC NP_001020018.1:n.-111_-110insAC
NM_003242.5:c.-111_-110insAC NP_003233.4:n.-111_-110insAC
XM_011534045.1:c.-12+180_-12+181insAC XP_011532347.1:n.-12+180_-12+181insAC
XM_011534045.3:c.-12+180_-12+181insAC XP_011532347.1:n.-12+180_-12+181insAC
NM_003242.6:c.-111_-110insAC MANE Select NP_003233.4:n.-111_-110insAC