Canonical Allele Identifier: CA2585296389

Gene: TGFB1

Linked Data

• gnomAD v4: 19-41342163-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342163G>C , CM000681.2:g.41342163G>C	GRCh38
NC_000019.9:g.41848068G>C , CM000681.1:g.41848068G>C	GRCh37
NC_000019.8:g.46539908G>C	NCBI36
NG_013364.1:g.16764C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000221930.6:c.712+7C>G MANE Select	ENSP00000221930.4:n.712+7C>G
ENST00000600196.2:c.712+7C>G	ENSP00000504008.1:n.712+7C>G
ENST00000677934.1:c.634+2584C>G	ENSP00000504769.1:n.634+2584C>G
ENST00000221930.5:c.712+7C>G	ENSP00000221930.4:n.712+7C>G
ENST00000597453.1:n.250C>G
ENST00000600196.1:n.172+7C>G
NM_000660.5:c.712+7C>G	NP_000651.3:n.712+7C>G
XM_011527242.1:c.712+7C>G	XP_011525544.1:n.712+7C>G
NM_000660.6:c.712+7C>G	NP_000651.3:n.712+7C>G
XM_011527242.2:c.712+7C>G	XP_011525544.1:n.712+7C>G
NM_000660.7:c.712+7C>G MANE Select	NP_000651.3:n.712+7C>G