Canonical Allele Identifier: CA405999309

Gene: TGFB1

Linked Data

• dbSNP Id: rs1599888665
• MyVariant Identifiers: chr19:g.41847821T>G (hg19) ; chr19:g.41341916T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41341916T>G , CM000681.2:g.41341916T>G	GRCh38
NC_000019.9:g.41847821T>G , CM000681.1:g.41847821T>G	GRCh37
NC_000019.8:g.46539661T>G	NCBI36
NG_013364.1:g.17011A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.827A>C MANE Select	ENSP00000221930.4:p.His276Pro
ENST00000600196.2:c.712+254A>C	ENSP00000504008.1:n.712+254A>C
ENST00000677934.1:c.634+2831A>C	ENSP00000504769.1:n.634+2831A>C
ENST00000221930.5:c.827A>C	ENSP00000221930.4:p.His276Pro
ENST00000598758.5:c.115A>C
ENST00000600196.1:n.172+254A>C
NM_000660.5:c.827A>C	NP_000651.3:p.His276Pro
XM_011527242.1:c.830A>C	XP_011525544.1:p.His277Pro
NM_000660.6:c.827A>C	NP_000651.3:p.His276Pro
XM_011527242.2:c.830A>C	XP_011525544.1:p.His277Pro
NM_000660.7:c.827A>C MANE Select	NP_000651.3:p.His276Pro