Canonical Allele Identifier: CA633167491

Gene: TGFB1

Linked Data

• dbSNP Id: rs2038137951
• gnomAD v2: 19-41854034-T-TA
• gnomAD v3: 19-41348129-T-TA
• gnomAD v4: 19-41348129-T-TA
• MyVariant Identifiers: chr19:g.41854035delinsAC (hg19) ; chr19:g.41348130delinsAC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41348129_41348130insA , CM000681.2:g.41348129_41348130insA	GRCh38
NC_000019.9:g.41854034_41854035insA , CM000681.1:g.41854034_41854035insA	GRCh37
NC_000019.8:g.46545874_46545875insA	NCBI36
NG_013364.1:g.10797_10798insT

Transcript Alleles

HGVS	Amino-acid change
ENST00000221930.6:c.516+165_516+166insT MANE Select	ENSP00000221930.4:n.516+165_516+166insT
ENST00000600196.2:c.516+165_516+166insT	ENSP00000504008.1:n.516+165_516+166insT
ENST00000677934.1:c.516+165_516+166insT	ENSP00000504769.1:n.516+165_516+166insT
ENST00000221930.5:c.516+165_516+166insT	ENSP00000221930.4:n.516+165_516+166insT
ENST00000597453.1:n.47+165_47+166insT
NM_000660.5:c.516+165_516+166insT	NP_000651.3:n.516+165_516+166insT
XM_011527242.1:c.516+165_516+166insT	XP_011525544.1:n.516+165_516+166insT
NM_000660.6:c.516+165_516+166insT	NP_000651.3:n.516+165_516+166insT
XM_011527242.2:c.516+165_516+166insT	XP_011525544.1:n.516+165_516+166insT
NM_000660.7:c.516+165_516+166insT MANE Select	NP_000651.3:n.516+165_516+166insT