Canonical Allele Identifier: CA351830497
Gene: TGFBR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30606906G>C , CM000665.2:g.30606906G>C GRCh38
NC_000003.11:g.30648398G>C , CM000665.1:g.30648398G>C GRCh37
NC_000003.10:g.30623402G>C NCBI36
NG_007490.1:g.5405G>C , LRG_779:g.5405G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.23G>C MANE Select ENSP00000295754.5:p.Gly8Ala
ENST00000295754.9:c.23G>C ENSP00000295754.5:p.Gly8Ala
ENST00000359013.4:c.23G>C ENSP00000351905.4:p.Gly8Ala
NM_001024847.2:c.23G>C , LRG_779t1:c.23G>C NP_001020018.1:p.Gly8Ala
NM_003242.5:c.23G>C NP_003233.4:p.Gly8Ala
XM_011534045.1:c.-12+313G>C XP_011532347.1:n.-12+313G>C
XM_011534045.3:c.-12+313G>C XP_011532347.1:n.-12+313G>C
NM_003242.6:c.23G>C MANE Select NP_003233.4:p.Gly8Ala