Canonical Allele Identifier: CA507689700

Gene: TGFB1

Linked Data

• ClinVar Variation Id: 799157
• ClinVar RCV Id: RCV000982739
• dbSNP Id: rs1479748627
• gnomAD v2: 19-41848124-G-A
• gnomAD v3: 19-41342219-G-A
• gnomAD v4: 19-41342219-G-A
• MyVariant Identifiers: chr19:g.41848124G>A (hg19) ; chr19:g.41342219G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342219G>A , CM000681.2:g.41342219G>A	GRCh38
NC_000019.9:g.41848124G>A , CM000681.1:g.41848124G>A	GRCh37
NC_000019.8:g.46539964G>A	NCBI36
NG_013364.1:g.16708C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000221930.6:c.663C>T MANE Select	ENSP00000221930.4:p.Ala221=
ENST00000600196.2:c.663C>T	ENSP00000504008.1:p.Ala221=
ENST00000677934.1:c.634+2528C>T	ENSP00000504769.1:n.634+2528C>T
ENST00000221930.5:c.663C>T	ENSP00000221930.4:p.Ala221=
ENST00000597453.1:n.194C>T
ENST00000600196.1:n.123C>T
NM_000660.5:c.663C>T	NP_000651.3:p.Ala221=
XM_011527242.1:c.663C>T	XP_011525544.1:p.Ala221=
NM_000660.6:c.663C>T	NP_000651.3:p.Ala221=
XM_011527242.2:c.663C>T	XP_011525544.1:p.Ala221=
NM_000660.7:c.663C>T MANE Select	NP_000651.3:p.Ala221=