Canonical Allele Identifier: CA71502517

Gene: TGFBR2

Linked Data

• dbSNP Id: rs947695219
• MyVariant Identifiers: chr3:g.30691029C>A (hg19) ; chr3:g.30649537C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30649537C>A , CM000665.2:g.30649537C>A	GRCh38
NC_000003.11:g.30691029C>A , CM000665.1:g.30691029C>A	GRCh37
NC_000003.10:g.30666033C>A	NCBI36
NG_007490.1:g.48036C>A , LRG_779:g.48036C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.264-733C>A MANE Select	ENSP00000295754.5:n.264-733C>A
ENST00000672866.1:n.1860-733C>A
ENST00000673250.1:n.388-733C>A
ENST00000295754.9:c.264-733C>A	ENSP00000295754.5:n.264-733C>A
ENST00000359013.4:c.339-733C>A	ENSP00000351905.4:n.339-733C>A
NM_001024847.2:c.339-733C>A , LRG_779t1:c.339-733C>A	NP_001020018.1:n.339-733C>A
NM_003242.5:c.264-733C>A	NP_003233.4:n.264-733C>A
XM_011534043.1:c.291-733C>A	XP_011532345.1:n.291-733C>A
XM_011534044.1:c.216-733C>A	XP_011532346.1:n.216-733C>A
XM_011534045.1:c.159-733C>A	XP_011532347.1:n.159-733C>A
XM_011534043.2:c.291-733C>A	XP_011532345.1:n.291-733C>A
XM_011534045.3:c.159-733C>A	XP_011532347.1:n.159-733C>A
XM_017007106.1:c.159-733C>A	XP_016862595.1:n.159-733C>A
NM_003242.6:c.264-733C>A MANE Select	NP_003233.4:n.264-733C>A