Canonical Allele Identifier: CA351808887

Gene: TGFBR2

Linked Data

• dbSNP Id: rs2125438757
• MyVariant Identifiers: chr3:g.30715606G>C (hg19) ; chr3:g.30674114G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30674114G>C , CM000665.2:g.30674114G>C	GRCh38
NC_000003.11:g.30715606G>C , CM000665.1:g.30715606G>C	GRCh37
NC_000003.10:g.30690610G>C	NCBI36
NG_007490.1:g.72613G>C , LRG_779:g.72613G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295754.10:c.1264G>C MANE Select	ENSP00000295754.5:p.Ala422Pro
ENST00000672866.1:n.2860G>C
ENST00000673203.1:n.142G>C
ENST00000295754.9:c.1264G>C	ENSP00000295754.5:p.Ala422Pro
ENST00000359013.4:c.1339G>C	ENSP00000351905.4:p.Ala447Pro
NM_001024847.2:c.1339G>C , LRG_779t1:c.1339G>C	NP_001020018.1:p.Ala447Pro
NM_003242.5:c.1264G>C	NP_003233.4:p.Ala422Pro
XM_011534043.1:c.1291G>C	XP_011532345.1:p.Ala431Pro
XM_011534044.1:c.1216G>C	XP_011532346.1:p.Ala406Pro
XM_011534045.1:c.1159G>C	XP_011532347.1:p.Ala387Pro
XM_011534043.2:c.1291G>C	XP_011532345.1:p.Ala431Pro
XM_011534045.3:c.1159G>C	XP_011532347.1:p.Ala387Pro
XM_017007106.1:c.1159G>C	XP_016862595.1:p.Ala387Pro
NM_003242.6:c.1264G>C MANE Select	NP_003233.4:p.Ala422Pro