Canonical Allele Identifier: CA351830629
Gene: TGFBR2 HGNC NCBI

Linked Data

dbSNP Id: rs2125438839

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30606969A>T , CM000665.2:g.30606969A>T GRCh38
NC_000003.11:g.30648461A>T , CM000665.1:g.30648461A>T GRCh37
NC_000003.10:g.30623465A>T NCBI36
NG_007490.1:g.5468A>T , LRG_779:g.5468A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.86A>T MANE Select ENSP00000295754.5:p.Gln29Leu
ENST00000295754.9:c.86A>T ENSP00000295754.5:p.Gln29Leu
ENST00000359013.4:c.86A>T ENSP00000351905.4:p.Gln29Leu
NM_001024847.2:c.86A>T , LRG_779t1:c.86A>T NP_001020018.1:p.Gln29Leu
NM_003242.5:c.86A>T NP_003233.4:p.Gln29Leu
XM_011534045.1:c.-12+376A>T XP_011532347.1:n.-12+376A>T
XM_011534045.3:c.-12+376A>T XP_011532347.1:n.-12+376A>T
NM_003242.6:c.86A>T MANE Select NP_003233.4:p.Gln29Leu