Canonical Allele Identifier: CA351830636
Gene: TGFBR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.30648464A>C (hg19) chr3:g.30606972A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30606972A>C , CM000665.2:g.30606972A>C GRCh38
NC_000003.11:g.30648464A>C , CM000665.1:g.30648464A>C GRCh37
NC_000003.10:g.30623468A>C NCBI36
NG_007490.1:g.5471A>C , LRG_779:g.5471A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000295754.10:c.89A>C MANE Select ENSP00000295754.5:p.Lys30Thr
ENST00000295754.9:c.89A>C ENSP00000295754.5:p.Lys30Thr
ENST00000359013.4:c.89A>C ENSP00000351905.4:p.Lys30Thr
NM_001024847.2:c.89A>C , LRG_779t1:c.89A>C NP_001020018.1:p.Lys30Thr
NM_003242.5:c.89A>C NP_003233.4:p.Lys30Thr
XM_011534045.1:c.-12+379A>C XP_011532347.1:n.-12+379A>C
XM_011534045.3:c.-12+379A>C XP_011532347.1:n.-12+379A>C
NM_003242.6:c.89A>C MANE Select NP_003233.4:p.Lys30Thr
Search 100 bp 5'
Search 100 bp 3'