Canonical Allele Identifier: CA72289918
Gene: TGFBR2 HGNC NCBI

Linked Data

dbSNP Id: rs753070840
MyVariant Identifiers: chr3:g.30648100C>G (hg19) chr3:g.30606608C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30606608C>G , CM000665.2:g.30606608C>G GRCh38
NC_000003.11:g.30648100C>G , CM000665.1:g.30648100C>G GRCh37
NC_000003.10:g.30623104C>G NCBI36
NG_007490.1:g.5107C>G , LRG_779:g.5107C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.-276C>G MANE Select ENSP00000295754.5:n.-276C>G
ENST00000295754.9:c.-276C>G ENSP00000295754.5:n.-276C>G
ENST00000359013.4:c.-276C>G ENSP00000351905.4:n.-276C>G
NM_001024847.2:c.-276C>G , LRG_779t1:c.-276C>G NP_001020018.1:n.-276C>G
NM_003242.5:c.-276C>G NP_003233.4:n.-276C>G
XM_011534045.1:c.-12+15C>G XP_011532347.1:n.-12+15C>G
XM_011534045.3:c.-12+15C>G XP_011532347.1:n.-12+15C>G
NM_003242.6:c.-276C>G MANE Select NP_003233.4:n.-276C>G
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