Canonical Allele Identifier: CA26699917

Gene: TGFBR3

Linked Data

• dbSNP Id: rs375630368
• gnomAD v2: 1-92194296-C-T
• gnomAD v3: 1-91728739-C-T
• gnomAD v4: 1-91728739-C-T
• MyVariant Identifiers: chr1:g.92194296C>T (hg19) ; chr1:g.91728739C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.91728739C>T , CM000663.2:g.91728739C>T	GRCh38
NC_000001.10:g.92194296C>T , CM000663.1:g.92194296C>T	GRCh37
NC_000001.9:g.91966884C>T	NCBI36
NG_027757.1:g.182264G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000212355.9:c.738-933G>A MANE Select	ENSP00000212355.4:n.738-933G>A
ENST00000212355.8:c.738-933G>A	ENSP00000212355.4:n.738-933G>A
ENST00000370399.6:c.738-933G>A	ENSP00000359426.2:n.738-933G>A
ENST00000465892.6:c.738-933G>A	ENSP00000432638.1:n.738-933G>A
ENST00000468996.2:n.540-933G>A
ENST00000525962.5:c.738-933G>A	ENSP00000436127.1:n.738-933G>A
ENST00000532540.5:c.*685-933G>A	ENSP00000434994.1:n.*685-933G>A
ENST00000533089.5:c.*705-933G>A	ENSP00000433477.1:n.*705-933G>A
NM_001195683.1:c.738-933G>A	NP_001182612.1:n.738-933G>A
NM_001195684.1:c.738-933G>A	NP_001182613.1:n.738-933G>A
NM_003243.4:c.738-933G>A	NP_003234.2:n.738-933G>A
NR_036634.1:n.1350-933G>A
XM_006710867.1:c.738-933G>A	XP_006710930.1:n.738-933G>A
XM_006710868.1:c.738-933G>A	XP_006710931.1:n.738-933G>A
XM_011542058.1:c.72-933G>A	XP_011540360.1:n.72-933G>A
XM_006710867.2:c.738-933G>A	XP_006710930.1:n.738-933G>A
NM_003243.5:c.738-933G>A MANE Select	NP_003234.2:n.738-933G>A
NM_001195683.2:c.738-933G>A	NP_001182612.1:n.738-933G>A
NR_036634.2:n.1222-933G>A