Canonical Allele Identifier: CA882316865

Gene: TGFB1

Linked Data

• dbSNP Id: rs1489248131
• gnomAD v3: 19-41342399-T-TC
• gnomAD v4: 19-41342399-T-TC
• MyVariant Identifiers: chr19:g.41848304_41848305insC (hg19) ; chr19:g.41342399_41342400insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342399_41342400insC , CM000681.2:g.41342399_41342400insC	GRCh38
NC_000019.9:g.41848304_41848305insC , CM000681.1:g.41848304_41848305insC	GRCh37
NC_000019.8:g.46540144_46540145insC	NCBI36
NG_013364.1:g.16527_16528insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.635-153_635-152insG MANE Select	ENSP00000221930.4:n.635-153_635-152insG
ENST00000600196.2:c.635-153_635-152insG	ENSP00000504008.1:n.635-153_635-152insG
ENST00000677934.1:c.634+2347_634+2348insG	ENSP00000504769.1:n.634+2347_634+2348insG
ENST00000221930.5:c.635-153_635-152insG	ENSP00000221930.4:n.635-153_635-152insG
ENST00000597453.1:n.166-153_166-152insG
ENST00000600196.1:n.95-153_95-152insG
NM_000660.5:c.635-153_635-152insG	NP_000651.3:n.635-153_635-152insG
XM_011527242.1:c.635-153_635-152insG	XP_011525544.1:n.635-153_635-152insG
NM_000660.6:c.635-153_635-152insG	NP_000651.3:n.635-153_635-152insG
XM_011527242.2:c.635-153_635-152insG	XP_011525544.1:n.635-153_635-152insG
NM_000660.7:c.635-153_635-152insG MANE Select	NP_000651.3:n.635-153_635-152insG