Canonical Allele Identifier: CA405998419

Gene: TGFB1

Linked Data

• gnomAD v4: 19-41332183-T-C
• MyVariant Identifiers: chr19:g.41838088T>C (hg19) ; chr19:g.41332183T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41332183T>C , CM000681.2:g.41332183T>C	GRCh38
NC_000019.9:g.41838088T>C , CM000681.1:g.41838088T>C	GRCh37
NC_000019.8:g.46529928T>C	NCBI36
NG_013364.1:g.26744A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.959A>G MANE Select	ENSP00000221930.4:p.Asn320Ser
ENST00000600196.2:c.811A>G	ENSP00000504008.1:p.Thr271Ala
ENST00000677934.1:c.733A>G	ENSP00000504769.1:p.Thr245Ala
ENST00000221930.5:c.959A>G	ENSP00000221930.4:p.Asn320Ser
ENST00000598758.5:c.247A>G
ENST00000600196.1:n.271A>G
NM_000660.5:c.959A>G	NP_000651.3:p.Asn320Ser
XM_011527242.1:c.962A>G	XP_011525544.1:p.Asn321Ser
NM_000660.6:c.959A>G	NP_000651.3:p.Asn320Ser
XM_011527242.2:c.962A>G	XP_011525544.1:p.Asn321Ser
NM_000660.7:c.959A>G MANE Select	NP_000651.3:p.Asn320Ser