Canonical Allele Identifier: CA2696352631

Gene: TGFBR3

Linked Data

• dbSNP Id: rs2100806333

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.91728701C>A , CM000663.2:g.91728701C>A	GRCh38
NC_000001.10:g.92194258C>A , CM000663.1:g.92194258C>A	GRCh37
NC_000001.9:g.91966846C>A	NCBI36
NG_027757.1:g.182302G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000212355.9:c.738-895G>T MANE Select	ENSP00000212355.4:n.738-895G>T
ENST00000212355.8:c.738-895G>T	ENSP00000212355.4:n.738-895G>T
ENST00000370399.6:c.738-895G>T	ENSP00000359426.2:n.738-895G>T
ENST00000465892.6:c.738-895G>T	ENSP00000432638.1:n.738-895G>T
ENST00000468996.2:n.540-895G>T
ENST00000525962.5:c.738-895G>T	ENSP00000436127.1:n.738-895G>T
ENST00000532540.5:c.*685-895G>T	ENSP00000434994.1:n.*685-895G>T
ENST00000533089.5:c.*705-895G>T	ENSP00000433477.1:n.*705-895G>T
NM_001195683.1:c.738-895G>T	NP_001182612.1:n.738-895G>T
NM_001195684.1:c.738-895G>T	NP_001182613.1:n.738-895G>T
NM_003243.4:c.738-895G>T	NP_003234.2:n.738-895G>T
NR_036634.1:n.1350-895G>T
XM_006710867.1:c.738-895G>T	XP_006710930.1:n.738-895G>T
XM_006710868.1:c.738-895G>T	XP_006710931.1:n.738-895G>T
XM_011542058.1:c.72-895G>T	XP_011540360.1:n.72-895G>T
XM_006710867.2:c.738-895G>T	XP_006710930.1:n.738-895G>T
NM_003243.5:c.738-895G>T MANE Select	NP_003234.2:n.738-895G>T
NM_001195683.2:c.738-895G>T	NP_001182612.1:n.738-895G>T
NR_036634.2:n.1222-895G>T