Canonical Allele Identifier: CA2585296356

Gene: TGFB1

Linked Data

• gnomAD v4: 19-41342049-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342049C>G , CM000681.2:g.41342049C>G	GRCh38
NC_000019.9:g.41847954C>G , CM000681.1:g.41847954C>G	GRCh37
NC_000019.8:g.46539794C>G	NCBI36
NG_013364.1:g.16878G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.713-19G>C MANE Select	ENSP00000221930.4:n.713-19G>C
ENST00000600196.2:c.712+121G>C	ENSP00000504008.1:n.712+121G>C
ENST00000677934.1:c.634+2698G>C	ENSP00000504769.1:n.634+2698G>C
ENST00000221930.5:c.713-19G>C	ENSP00000221930.4:n.713-19G>C
ENST00000597453.1:n.364G>C
ENST00000600196.1:n.172+121G>C
NM_000660.5:c.713-19G>C	NP_000651.3:n.713-19G>C
XM_011527242.1:c.713-16G>C	XP_011525544.1:n.713-16G>C
NM_000660.6:c.713-19G>C	NP_000651.3:n.713-19G>C
XM_011527242.2:c.713-16G>C	XP_011525544.1:n.713-16G>C
NM_000660.7:c.713-19G>C MANE Select	NP_000651.3:n.713-19G>C