Canonical Allele Identifier: CA406003696
Gene: TGFB1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.41854300T>G (hg19) chr19:g.41348395T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41348395T>G , CM000681.2:g.41348395T>G GRCh38
NC_000019.9:g.41854300T>G , CM000681.1:g.41854300T>G GRCh37
NC_000019.8:g.46546140T>G NCBI36
NG_013364.1:g.10532A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.416A>C MANE Select ENSP00000221930.4:p.Glu139Ala
ENST00000600196.2:c.416A>C ENSP00000504008.1:p.Glu139Ala
ENST00000677934.1:c.416A>C ENSP00000504769.1:p.Glu139Ala
ENST00000221930.5:c.416A>C ENSP00000221930.4:p.Glu139Ala
NM_000660.5:c.416A>C NP_000651.3:p.Glu139Ala
XM_011527242.1:c.416A>C XP_011525544.1:p.Glu139Ala
NM_000660.6:c.416A>C NP_000651.3:p.Glu139Ala
XM_011527242.2:c.416A>C XP_011525544.1:p.Glu139Ala
NM_000660.7:c.416A>C MANE Select NP_000651.3:p.Glu139Ala
Search 100 bp 5'
Search 100 bp 3'