Canonical Allele Identifier: CA406003523

Gene: TGFB1

Linked Data

• MyVariant Identifiers: chr19:g.41854221C>G (hg19) ; chr19:g.41348316C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41348316C>G , CM000681.2:g.41348316C>G	GRCh38
NC_000019.9:g.41854221C>G , CM000681.1:g.41854221C>G	GRCh37
NC_000019.8:g.46546061C>G	NCBI36
NG_013364.1:g.10611G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.495G>C MANE Select	ENSP00000221930.4:p.Glu165Asp
ENST00000600196.2:c.495G>C	ENSP00000504008.1:p.Glu165Asp
ENST00000677934.1:c.495G>C	ENSP00000504769.1:p.Glu165Asp
ENST00000221930.5:c.495G>C	ENSP00000221930.4:p.Glu165Asp
ENST00000597453.1:n.26G>C
NM_000660.5:c.495G>C	NP_000651.3:p.Glu165Asp
XM_011527242.1:c.495G>C	XP_011525544.1:p.Glu165Asp
NM_000660.6:c.495G>C	NP_000651.3:p.Glu165Asp
XM_011527242.2:c.495G>C	XP_011525544.1:p.Glu165Asp
NM_000660.7:c.495G>C MANE Select	NP_000651.3:p.Glu165Asp